Chlorofluorobenzene liquid crystal compound, liquid crystal composition, and liquid crystal display device

ABSTRACT

Such a liquid crystal compound is provided that has stability to heat, light and so forth, has a nematic phase in a wide temperature range, has a small viscosity, a suitable optical anisotropy, and suitable elastic constants K 33  and K 11  (K 33 : bend elastic constant, K 11 : splay elastic constant), and has suitable negative dielectric anisotropy and excellent compatibility with other liquid crystal compounds. A liquid crystal composition containing the liquid crystal compound, and a liquid crystal display device containing the liquid crystal composition are also provided. 
     The liquid crystal compound is represented by one of formulas (a) to (d), the liquid crystal composition contains the liquid crystal compound, and the liquid crystal display device contains the liquid crystal composition: 
                         
wherein Ra and Rb are independently linear alkyl or linear alkoxy, rings A 1 , A 2 , B and C are independently trans-1,4-cyclohexylene or 1,4-phenylene, Z 11 , Z 12 , Z 2  and Z 3  are independently a single bond or alkylene, and one of X 1  and X 2  is fluorine, and the other thereof is chlorine.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a divisional application of, and claims the prioritybenefit of, U.S. application Ser. No. 11/368,305 filed on Mar. 3, 2006,which claims the priority benefit of Japan application No. 2005-59154,filed on Mar. 3, 2005. All disclosures of these prior applications areincorporated herein by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a liquid crystal compound, a liquidcrystal composition, and a liquid crystal display device. Morespecifically, the invention relates to a chlorofluorobenzene derivative,which is a liquid crystal compound, a liquid crystal compositioncontaining the compound and having a nematic phase, and a liquid crystaldisplay device containing the composition.

2. Related Art

A liquid crystal display device utilizes optical anisotropy anddielectric anisotropy inherent to a liquid crystal compound (whichmeans, in the invention, a generic term for a compound having a liquidcrystal phase such as a nematic phase, a smectic phase and so forth, andalso for a compound having no liquid crystal phase but being useful as acomponent of a composition). On a liquid crystal display device, variousmodes including a phase change (PC) mode, a twisted nematic (TN) mode, asuper twisted nematic (STN) mode, a bistable twisted nematic (BTN) mode,an electrically controlled birefringence (ECB) mode, an opticallycompensated bend (OCB) mode, an in-plane switching (IPS) mode, avertical alignment (VA) mode, and so forth.

Among these operation modes, an ECB mode, an ISP mode, a VA mode and soforth are operation modes utilizing vertical orientation of liquidcrystal molecules, and it has been known that in particular an IPS modeand a VA mode are capable of improving the narrow viewing angle, whichis a problem of the conventional display modes, such as a TN mode, anSTN mode and so forth.

As a component of a liquid crystal composition having a negativedielectric anisotropy capable of being used in a liquid crystal displaydevice of these operation modes, a large number of such liquid crystalcompounds have been investigated that hydrogen on a benzene ring isreplaced by fluorine (see, for example, JP H2-503441 A/1990 and JPH02-4725 A/1990).

For example, a compound (A) represented by the following structuralformula has been investigated (see, for example, JP H2-503441 A/1990).However, a compound, in which hydrogen on a benzene ring is replaced byfluorine, represented by the compound (A) is poor in compatibility withother compounds in a low temperature region.

As a compound, in which hydrogen on a benzene ring is substituted bychlorine and fluorine, for example, a compound (B) represented by thefollowing structural formula has been reported (see, for example, WO98/23561 A/1998). However, the compound (B) does not have a high clearpoint and has a large viscosity.

As a compound, in which hydrogen on a benzene ring is substituted bychlorine, for example, a compound (C) represented by the followingstructural formula has been reported (see, for example, MolecularCrystals and Liquid Crystals, vol. 260, pp. 227-240 (1995)). However,the compound (C) has a significantly narrow range (mesomorphic range)where the compound shows liquid crystallinity and has a small negativedielectric anisotropy.

As chiral dopants in liquid-crystalline media for electro-opticaldisplays, for example, a compound (D) represented by the followingstructural formula has been reported (see, for example, JP H10/158,652A/1998). However, the compound (D) has a significantly narrow range(mesomorphic range) where the compound shows liquid crystallinity.

Therefore, a liquid crystal display device having such an operation modeas an IPS mode, a VA mode and so forth still has problems in comparisonto CRT, and improvement in response time, improvement in contrast, anddecrease in driving voltage are demanded.

The liquid crystal display device driven in an IPS mode or a VA mode isconstituted mainly by a liquid crystal composition having a negativedielectric anisotropy, and in order to improve the aforementionedcharacteristics, a liquid crystal compound contained in the liquidcrystal composition is demanded to have the following characteristics(1) to (8).

Namely, the compound:

(1) is chemically stable and physically stable,

(2) has high clear point (transition temperature between a liquidcrystal phase and an isotropic phase),

(3) has low minimum temperature of a liquid crystal phase (such as anematic phase, a smectic phase and so forth), particularly a low minimumtemperature of a nematic phase,

(4) has small viscosity,

(5) has suitable optical anisotropy,

(6) has suitable negative dielectric anisotropy,

(7) has suitable elastic constants K₃₃ and K₁₁ (K₃₃: bend elasticconstant, K₁₁: splay elastic constant), and

(8) is excellent in compatibility with other compounds.

In the case where a composition containing a chemically and physicallystable compound as in (1) is used in a display device, a voltage holdingratio can be increased.

In the case of a composition containing a liquid crystal compound havinga high clear point or a low minimum temperature of a liquid crystalphase as in (2) or (3), the temperature range of a nematic phase can beenhanced, whereby the display device can be used in a wide temperaturerange.

In the case where a composition containing a compound having smallviscosity as in (4) or a compound having suitable elastic constants K₃₃and K₁₁ as in (7) is used in a display device, the response time can beimproved. In the case where a composition containing a compound havingsuitable optical anisotropy as in (5) is used in a display device, thedisplay device can be improved in contrast.

A liquid crystal composition containing a liquid crystal compound havinga negatively large dielectric anisotropy has low threshold voltage, andtherefore, in the case of a display device using a compositioncontaining a compound having suitable negative dielectric anisotropy asin (6), the display device can have a low driving voltage and smallelectric power consumption. In the case where a composition containing acompound having suitable elastic constant K₃₃ as in (7) is used in adisplay device, the driving voltage of the display device can becontrolled, and the electric power consumption thereof can also becontrolled.

A liquid crystal compound is generally used as a composition obtained bymixing with other many liquid crystal compounds for exhibiting suchcharacteristics that are difficult to obtain with a sole compound.Therefore, a liquid crystal compound used in a display device desirablyhas good compatibility with other compounds as in (8). A display deviceis used in a wide temperature range including temperatures belowfreezing point in some cases, and therefore, a compound used in thecomposition desirably has good compatibility in a low temperature rangein some cases.

SUMMARY OF THE INVENTION

The invention concerns a liquid crystal compound represented by one offormulas (a) to (d):

wherein Ra and Rb are independently hydrogen or linear alkyl having 1 to10 carbons, provided that in the alkyl, —CH₂— may be replaced by —O—,—(CH₂)₂— may be replaced by —CH═CH—, and hydrogen may be replaced by ahalogen; rings A¹, A², B and C are independently trans-1,4-cyclohexyleneor 1,4-phenylene; Z¹¹, Z¹², Z² and Z³ are independently a single bond oralkylene having 2 or 4 carbons, provided that in the alkylene, —CH₂— maybe replaced by —O— and —(CH₂)₂— may be replaced by —CH═CH—; and one ofX₁ and X₂ is fluorine, and the other thereof is chlorine, provided that:

in a case where:

-   -   in formula (a), rings B and C are trans-1,4-cyclohexylene, and        Z² and Z³ are a single bond,    -   in formula (b), rings A¹ and B are trans-1,4-cyclohexylene, Z¹¹        is a single bond, and Z² is —CH₂O—, and    -   in formula (d), rings A¹, A² and B are trans-1,4-cyclohexylene,        Z¹¹ and Z¹² are a single bond, and Z² is a single bond or        —CH₂O—,

Rb is one of linear alkoxy having 1 to 9 carbons, linear alkoxyalkylhaving 2 to 9 carbons, linear alkenyl having 2 to 10 carbons, linearalkenyloxy having 2 to 9 carbons, linear fluoroalkyl having 1 to 10carbons, and linear fluoroalkoxy having 1 to 9 carbons.

The invention also concerns a liquid crystal composition comprising theliquid crystal compound.

The invention also concerns a liquid crystal display device comprising aliquid crystal composition comprising the liquid crystal compound.

DETAILED DESCRIPTION

A first object of the invention is to provide such a liquid crystalcompound that has stability to heat, light and so forth, has a nematicphase in a wide temperature range, has a small viscosity, a suitableoptical anisotropy, and suitable elastic constants K₃₃ and K₁₁, and hassuitable negative dielectric anisotropy and excellent compatibility withother liquid crystal compounds.

A second object of the invention is to provide such a liquid crystalcomposition containing the liquid crystal compound that has a lowviscosity, a suitable optical anisotropy, a suitable negative dielectricanisotropy, a low threshold voltage, a high maximum temperature of anematic phase (phase transition temperature between a nematic phase andan isotropic phase), and a low minimum temperature of a nematic phase.

A third object of the invention is to provide such a liquid crystaldisplay device containing the composition that has a short responsetime, a small electric power consumption, a small driving voltage, and alarge contrast, and can be used in a wide temperature range.

As a result of earnest investigations on the aforementioned problemsmade by the inventors, it has been found that:

a liquid crystal compound having a particular structure, in whichhydrogen on a benzene ring is replaced by chlorine and fluorine, hasstability to heat, light and so forth, has a nematic phase in a widetemperature range, has a small viscosity, a suitable optical anisotropy,and suitable elastic constants K₃₃ and K₁₁ (K₃₃: bend elastic constant,K₁₁: splay elastic constant), and has suitable negative dielectricanisotropy and excellent compatibility with other liquid crystalcompounds,

a liquid crystal composition containing the liquid crystal compound hasa low viscosity, a suitable optical anisotropy, a suitable negativedielectric anisotropy, a low threshold voltage, a high maximumtemperature of a nematic phase, and a low minimum temperature of anematic phase, and a liquid crystal display device containing thecomposition has a short response time, a small electric powerconsumption, a small driving voltage, and a large contrast, and can beused in a wide temperature range, and thus the invention has beencompleted.

The invention has the following features:

1. A liquid crystal compound represented by one of formulas (a) to (d):

wherein Ra and Rb are independently hydrogen or linear alkyl having 1 to10 carbons, provided that in the alkyl, —CH₂— may be replaced by —O—,—(CH₂)₂— may be replaced by —CH═CH—, and hydrogen may be replaced by ahalogen; rings A¹, A², B and C are independently trans-1,4-cyclohexyleneor 1,4-phenylene; Z¹¹, Z¹², Z² and Z³ are independently a single bond oralkylene having 2 or 4 carbons, provided that in the alkylene, —CH₂— maybe replaced by —O— and —(CH₂)₂— may be replaced by —CH═CH—; and one ofX₁ and X₂ is fluorine, and the other thereof is chlorine, provided that:

in a case where:

-   -   in formula (a), rings B and C are trans-1,4-cyclohexylene, and        Z² and Z³ are a single bond,    -   in formula (b), rings A¹ and B are trans-1,4-cyclohexylene, Z¹¹        is a single bond, and Z² is —CH₂O—, and    -   in formula (d), rings A¹, A² and B are trans-1,4-cyclohexylene,        Z¹¹ and Z¹² are a single bond, and Z² is a single bond or        —CH₂O—,

Rb is one of linear alkoxy having 1 to 9 carbons, linear alkoxyalkylhaving 2 to 9 carbons, linear alkenyl having 2 to 10 carbons, linearalkenyloxy having 2 to 9 carbons, linear fluoroalkyl having 1 to 10carbons, and linear fluoroalkoxy having 1 to 9 carbons.

2. A liquid crystal compound represented by one of formulas (a-1) to(d-1):

wherein Ra₁ and Rb₁ are independently linear alkyl having 1 to 10carbons, provided that in the alkyl, —CH₂— may be replaced by —O—,—(CH₂)₂— may be replaced by —CH═CH—, and hydrogen may be replaced by ahalogen; rings A¹, A² and B are independently trans-1,4-cyclohexylene or1,4-phenylene; Z¹¹, Z¹², Z² and Z³ are independently a single bond oralkylene having 2 or 4 carbons, provided that in the alkylene, —CH₂— maybe replaced by —O— and —(CH₂)₂— may be replaced by —CH═CH—; and one ofX₁ and X₂ is fluorine, and the other thereof is chlorine, provided that:

in a case where:

-   -   in formula (b-1), rings A¹ and B are trans-1,4-cyclohexylene,        Z¹¹ is a single bond, and Z² is —CH₂O—, and    -   in formula (d-1), rings A¹, A² and B are        trans-1,4-cyclohexylene, Z¹¹ and Z¹² are a single bond, and Z²        is a single bond or —CH₂O—,

Rb₁ is one of linear alkoxy having 1 to 9 carbons, linear alkoxyalkylhaving 2 to 9 carbons, linear alkenyl having 2 to 10 carbons, linearalkenyloxy having 2 to 9 carbons, linear fluoroalkyl having 1 to 10carbons, and linear fluoroalkoxy having 1 to 9 carbons. 3. The liquidcrystal compound according to item 2, wherein the compound representedby formula (a-1) or (b-1), wherein Ra₁ and Rb₁ are independently linearalkyl having 1 to 10 carbons, linear alkoxy having 1 to 9 carbons,linear alkoxyalkyl having 1 to 9 carbons, linear alkenyl having 2 to 10carbons, linear alkenyloxy having 2 to 9 carbons, linear fluoroalkylhaving 1 to 10 carbons or linear fluoroalkoxy having 1 to 9 carbons, andZ¹¹, Z¹², Z² and Z³ are independently a single bond, —(CH₂)₂—, —CH═CH—,—CH₂O— or —OCH₂—.

4. The liquid crystal compound according to item 2, wherein the compoundrepresented by formula (c-1) or (d-1), wherein Ra₁ and Rb₁ areindependently linear alkyl having 1 to 10 carbons, linear alkoxy having1 to 9 carbons, linear alkoxyalkyl having 1 to 9 carbons, linear alkenylhaving 2 to 10 carbons, linear fluoroalkyl having 1 to 10 carbons orlinear fluoroalkoxy having 1 to 9 carbons, and

Z¹¹, Z¹², Z² and Z³ are independently a single bond, —(CH₂)₂—, —CH═CH—,—CH₂O— or —OCH₂—.

5. The liquid crystal compound according to item 2, wherein the compoundrepresented by one of formulas (a-1) to (d-1), wherein Ra₁ is linearalkyl having 1 to 10 carbons or linear alkenyl having 2 to 10 carbons,Rb₁ is linear alkyl having 1 to 10 carbons or linear alkoxy having 1 to9 carbons, and Z¹¹, Z¹², Z² and Z³ are independently a single bond,—(CH₂)₂—, —CH═CH—, —CH₂O— or —OCH₂—.

6. The liquid crystal compound according to item 2, wherein the compoundrepresented by one of formulas (a-1) to (d-1), wherein Z¹¹, Z¹², Z² andZ³ are independently a single bond, —(CH₂)₂— or —CH═CH—.

7. The liquid crystal compound according to item 2, wherein the compoundrepresented by one of formulas (a-1) to (d-1), wherein Ra₁ is linearalkyl having 1 to 10 carbons or linear alkenyl having 2 to 10 carbons,Rb₁ is linear alkoxy having 1 to 9 carbons, Z¹¹, Z¹² and Z³ areindependently a single bond, —(CH₂)₂—, —CH═CH—, —CH₂O— or —OCH₂—, and Z²is —CH₂O—.

8. The liquid crystal compound according to any one of items 2 to 7,wherein the compound represented by one of formulas (a-1) to (d-1),wherein X₁ is fluorine, and X₂ is chlorine.

9. The liquid crystal compound according to any one of items 2 to 7,wherein the compound represented by one of formulas (a-1) to (d-1),wherein X₁ is chlorine, and X₂ is fluorine.

10. A liquid crystal compound represented by one of formulas (b-2-1) to(b-7-1):

wherein Ra₂ is linear alkyl having 1 to 10 carbons or linear alkenylhaving 2 to 10 carbons, Rb₂ is linear alkyl having 1 to 10 carbons orlinear alkoxy having 1 to 9 carbons, and the cyclohexylene ring istrans-1,4-cyclohexylene.

11. A liquid crystal compound represented by one of formulas (b-2-2) to(b-7-2):

wherein Ra₂ is linear alkyl having 1 to 10 carbons or linear alkenylhaving 2 to 10 carbons, Rb₂ is linear alkyl having 1 to 10 carbons orlinear alkoxy having 1 to 9 carbons, and the cyclohexylene ring istrans-1,4-cyclohexylene.

12. The liquid crystal compound according to item 10, wherein thecompound represented by one of formulas (b-2-1) to (b-7-1), wherein Ra₂is linear alkyl having 1 to 10 carbons, and Rb₂ is linear alkoxy having1 to 9 carbons.

13. The liquid crystal compound according to item 11, wherein thecompound represented by one of formulas (b-2-2) to (b-7-2), wherein Ra₂is linear alkyl having 1 to 10 carbons, and Rb₂ is linear alkoxy having1 to 9 carbons

14. A liquid crystal compound represented by one of formulas (b-8-1) to(b-10-1):

wherein Ra₃ is linear alkyl having 1 to 10 carbons or linear alkenylhaving 2 to 10 carbons, Rb₃ is linear alkoxy having 1 to 9 carbons, andthe cyclohexylene ring is trans-1,4-cyclohexylene.

15. A liquid crystal compound represented by one of formulas (b-8-2) to(b-10-2):

wherein Ra₃ is linear alkyl having 1 to 10 carbons or linear alkenylhaving 2 to 10 carbons, Rb₃ is linear alkoxy having 1 to 9 carbons, andthe cyclohexylene ring is trans-1,4-cyclohexylene.

16. The liquid crystal compound according to item 14, wherein thecompound represented by one of formulas (b-8-1) to (b-10-1), wherein Ra₃is linear alkyl having 1 to 10 carbons.

17. The liquid crystal compound according to item 15, wherein thecompound represented by one of formulas (b-8-2) to (b-10-2), wherein Ra₃is linear alkyl having 1 to 10 carbons.

18. A compound represented by formula (I) or (II):

wherein Rc is alkyl having 1 to 10 carbons, provided that in the alkyl,—CH₂— may be replaced by —O—, —(CH₂)₂— may be replaced by —CH═CH—, andhydrogen may be replaced by a halogen; and X₃ is bromine or iodine.

19. A compound represented by formula (II) or (IV) used as anintermediate compound of the liquid crystal compound according to anyone of items 1 to 17:

wherein Rd is linear alkyl having 1 to 10 carbons or linear alkoxyhaving 1 to 9 carbons, and X₃ is bromine or iodine.

20. A compound represented by formula (V) or (VI) used as anintermediate compound of the liquid crystal compound according to anyone of items 1 to 17:

wherein Re is linear alkyl having 1 to 10 carbons, provided that in thealkyl, —CH₂— may be replaced by —O—, —(CH₂)₂— may be replaced by—CH═CH—, and hydrogen may be replaced by a halogen.

21. A liquid crystal composition comprising the liquid crystal compoundaccording to any one of items 1 to 17.

22. A liquid crystal display device comprising a liquid crystalcomposition comprising the liquid crystal compound according to any oneof items 1 to 17.

The invention also concerns a liquid crystal composition containing thecompound, and a liquid crystal display device containing thecomposition.

The liquid crystal compound of the invention has stability to heat,light and so forth, has a nematic phase in a wide temperature range, hassmall viscosity, suitable optical anisotropy, and suitable elasticconstants K₃₃ and K₁₁ (K₃₃: bend elastic constant, K₁₁: splay elasticconstant), and has suitable negative dielectric anisotropy and excellentcompatibility with other liquid crystal compounds. In particular, thecompound of the invention is excellent in such points that the compoundhas suitable negative dielectric anisotropy and excellent compatibilitywith other liquid crystal compounds. The liquid crystal compound can beeasily produced by using an intermediate compound of the inventionhaving stability to heat, light and so forth capable of being used forwide variety of reactions.

The liquid crystal composition of the invention has low viscosity,suitable optical anisotropy, suitable negative dielectric anisotropy,low threshold voltage, high maximum temperature of nematic phase, andlow minimum temperature of nematic phase. In particular, the compositionof the invention is excellent in such points that since the liquidcrystal compound of the invention has suitable negative dielectricanisotropy and excellent compatibility with other liquid crystalcompounds, the compound of the invention can be used in a widecompositional range to prepare a liquid crystal composition havingsuitable negative dielectric anisotropy.

The liquid crystal display device containing the composition has shortresponse time, small electric power consumption, small driving voltage,and large contrast, and can be used in wide temperature range.Accordingly, the liquid crystal display device can be favorably appliedto a liquid crystal display device having such an operation mode as a PCmode, a TN mode, a STN mode, an ECB mode, an OCB mode, an IPS mode, a VAmode and so forth, and in particular, can be favorably applied to aliquid crystal display device having an IPS mode or a VA mode.

The invention will be described more specifically.

In the description, the content (percentage) of a compound means apercentage by weight (% by weight) based on the total weight of thecomposition.

(Liquid Crystal Compound)

The liquid crystal compounds of the invention have structuresrepresented by formulas (a) to (d) (hereinafter, the compounds arereferred to as a liquid crystal compound (1) as a generic term).

In the liquid crystal compound (1), Ra and Rb are independently hydrogenor linear alkyl having 1 to 10 carbons, provided that in the alkyl,—CH₂— may be replaced by —O—, and —(CH₂)₂— may be replaced by —CH═CH—.

For example, in the case where the linear alkyl is CH₃(CH₂)₃—, thelinear alkyl may be CH₃(CH₂)₂—, CH₃—O—(CH₂)₂—, CH₃—O—CH₂—O—, H₂C═CH—(CH₂)₂—, CH₃—CH═CH—CH₂— or CH₃—CH═CH—O—, which are obtained by replacing—CH₂— by —O—, or replacing —(CH₂)₂— by —CH═CH—.

In Ra and Rb, two or more —CH₂— may be replaced by —O—, but inconsideration of stability of the compound, a group having oxygens notadjacent to each other, such as CH₃—O—CH₂—O— is preferred in comparisonto a group having oxygens adjacent to each other, such as CH₃—O—O—CH₂—.

More specific examples of Ra and Rb include hydrogen, linear alkyl,linear alkoxyalkyl, linear alkoxyalkoxy, linear alkenyl, linearalkenyloxy, linear alkenyloxyalkyl and linear alkoxyalkenyl.

In these groups, one or more hydrogen may be replaced by a halogen, andpreferred examples of the halogen for replacing hydrogen includefluorine and chlorine.

In the groups, the alkyl chain is desirably a linear chain. In the casewhere the alkyl chain is a linear chain, the temperature range of theliquid crystal phase can be enhanced, and the viscosity thereof can bedecreased. In the case where one of Ra and Rb is an optically activegroup, it is useful as a chiral dopant, and the addition of the compoundprevents a reverse twisted domain from being formed in the liquidcrystal display device.

Desirable Ra and Rb are linear alkyl, linear alkoxy, linear alkoxyalkyl,linear alkenyl, linear fluoroalkyl or linear fluoroalkoxy, moredesirable Ra and Rb are linear alkyl, linear alkoxy, linear alkoxyalkyl,linear alkenyl, —CH₂F or —OCH₂F, and further desirable Ra and Rb arelinear alkyl, linear alkoxy or linear alkenyl.

In the case where Ra and Rb are the aforementioned groups, thetemperature range of the liquid crystal phase of the liquid crystalcompound can be enhanced.

The linear alkenyl has a desirable configuration of —CH═CH— depending onthe position of the double bond of the alkenyl.

In the alkenyl having a double bond at an odd number position, such as—CH═CHCH₃, —CH═CHC₂H₅, —CH═CHC₃H₇, —CH═CHC₄H₉, —C₂H₄═CH═CHCH₃ and—C₂H₄═CH═CHC₂H₅, the configuration is desirably a trans configuration.

In the linear alkenyl having a double bond at an even number position,such as —CH₂CH═CHCH₃, —CH₂CH═CHC₂H₅ and —CH₂CH═CHC₃H₇, the configurationis desirably a cis configuration. The alkenyl compound having theaforementioned configuration has a wide temperature range of the liquidcrystal phase, has large elastic constants K₃₃ and K₁₁ (K₃₃: bendelastic constant, K₁₁: splay elastic constant), and a small viscosity,and the addition of the compound to a liquid crystal compositionincreases a maximum temperature (TNI) of a nematic phase.

Specific examples of the linear alkyl include —CH₃, —C₂H₅, —C₃H₇, —C₄H₉,—C₅H₁₁, —C₆H₁₃ and —C₇H₁₅,

specific examples of the linear alkoxy include —OCH₃, —OC₂H₅, —OC₃H₇,—OC₄H₉, —OC₅H₁₁ and —OC₆H₁₃,

specific example of the linear alkoxyalkyl include —CH₂OCH₃, —CH₂OC₂H₅,—CH₂OC₃H₇, —(CH₂)₂OCH₃, —(CH₂)₂OC₂H₅, —(CH₂)₂OC₃H₇, —(CH₂)₃OCH₃,—(CH₂)₄OCH₃ and —(CH₂)₅OCH₃,

specific examples of the linear alkenyl include —CH═CH₂, —CH═CHCH₃,—CH₂CH═CH₂, —CH═CHC₂H₅, —CH₂CH═C HCH₃, —(CH₂)₂CH═CH₂, —CH═CHC₃H₇,—CH₂CH═CHC₂H₅, —(CH₂)₂CH═CHCH₃ and —(CH₂)₃CH═CH₂, and

specific examples of the linear alkenyloxy include —OCH₂CH═CH₂,—OCH₂CH═CHCH₃ and —OCH₂CH═CHC₂H₅.

Specific examples of the linear alkyl, in which hydrogen is replaced bya halogen, include —CH₂F, —CHF₂, —CF₃, —(CH₂)₂F, —CF₂CH₂F, —CF₂CHF₂,—CH₂CF₃, —CF₂CF₃, —(CH₂)₃F, —(CF₂)₂CF₃, —CF₂CHFCF₃ and —CHFCF₂CF₃,

specific examples of the linear alkoxy, in which hydrogen is replaced bya halogen, include —OCF₃, —OCHF₂, —OCH₂F, —OCF₂CF₃, —OCF₂CHF₂,—OCF₂CH₂F, —OCF₂CF₂CF₃, —OCF₂CHFCF₃ and —OCHFCF₂CF₃, and

specific examples of the linear alkenyl, in which hydrogen is replacedby a halogen, include —CH═CHF, —CH═CF₂, —CF═CHF, —CH═CHCH₂F, —CH═CHCF₃and —(CH₂)₂CH═CF₂.

Among the specific examples of Ra and Rb, —CH₃, —C₂H₅, —C₃H₇, —C₄H₉,—C₅H₁₁, —OCH₃, —OC₂H₅, —OC₃H₇, —OC₄H₉, —OC₅H₁₁, —CH₂OCH₃, —(CH₂)₂OCH₃,—(CH₂)₃OCH₃, —CH═CH₂, —CH═CHCH₃, —CH₂CH═CH₂, —CH═CHC₂H₅, —CH₂CH═CHCH₃,—(CH₂)₂CH═CH₂, —CH═CHC₃H₇, —CH₂CH═CHC₂H₅, —(CH₂)₂CH═CHCH₃,—(CH₂)₃CH═CH₂, —OCH₂CH═CH₂, —OCH₂CH═CHCH₃, —OCH₂CH═CHC₂H₅, —CF₃, —CHF₂,—CH₂F, —OCF₃, —OCHF₂, —OCH₂F, —OCF₂CF₃, —OCF₂CHF₂, —OCF₂CH₂F,—OCF₂CF₂CF₃, —OCF₂CHFCF₃ and —OCHFCF₂CF₃ are preferred,

—CH₃, —C₂H₅, —C₃H₇, —C₄H₉, —C₅H₁₁, —OCH₃, —OC₂H₅, —OC₃H₇, —OC₄H₉,—OC₅H₁₁, —CH₂OCH₃, —CH═CH₂, —CH═CHCH₃, —CH₂CH═CH₂, —CH═CHC₂H₅,—CH₂CH═CHCH₃, —(CH₂)₂CH═CH₂, —CH═CHC₃H₇, —CH₂CH═CHC₂H₅, —(CH₂)₂CH═CHCH₃,—(CH₂)₃CH═CH₂, —CHF₂ and —OCH₂F are more preferred, and

—CH₃, —C₂H₅, —C₃H₇, —C₄H₉, —C₅H₁₁, —OCH₃, —OC₂H₅, —OC₃H₇, —CH₂OCH₃,—CH═CH₂, —CH═CHCH₃, —(CH₂)₂CH═CH₂ and —(CH₂)₂CH═CHCH₃ are furtherpreferred.

Rings A¹, A², B and C are independently trans-1,4-cyclohexylene or1,4-phenylene.

In the case where at least two rings among these aretrans-1,4-cyclohexane, the optical anisotropy (Δn) and the viscosity canbe small, and the addition of the liquid crystal compound to a liquidcrystal composition increases the maximum temperature (TNI) of a nematicphase.

In the case where at least one ring among these is 1,4-phenylene, theoptical anisotropy (Δn) can be relatively large, and the orientationalorder parameter can be large.

In the case where at least two rings among these are 1,4-phenylene, theoptical anisotropy can be large.

Examples of Z¹¹, Z¹², Z² and Z³ include a single bond, —(CH₂)₂—, —CH₂O—,—OCH₂—, —CH═CH—, —(CH₂)₄—, —CH═CH—(CH₂)₂—, —CH₂—CH═CH—CH₂—,—(CH₂)₂—CH═CH—, —CH═CH—CH₂O— and —OC H₂—CH═CH—.

In the case where Z¹¹, Z¹², Z² and Z³ are a bonding group including—CH═CH—, —CH═CH— (CH₂)₂—, —(CH₂)₂—CH═CH—, —CH═CH—C H₂O— and—OCH₂—CH═CH—, the configuration of the other groups with respect to thedouble bond is desirably a trans configuration, and in the case wherethey are —CH₂—CH═CH—CH₂—, the configuration is desirably a cisconfiguration. According to the configurations of the liquid crystalcompound, the temperature range of the liquid crystal phase can beenhanced, and the elastic constants K₃₃ can be increased. The additionof the liquid crystal compound to a liquid crystal composition increasesthe maximum temperature (T_(NI)) of a nematic phase.

Among the examples of Z¹¹, Z¹², Z² and Z³, a single bond, —(CH₂)₂—,—CH₂O—, —OCH₂—, —CH═CH— and —(CH₂)₄— are preferred,

a single bond, —(CH₂)₂—, —CH₂O—, —OCH₂— and —CH═CH— are more preferred,and

a single bond and —(CH₂)₂— are further preferred.

In the case where Z¹¹, Z¹², Z² and Z³ are a single bond, —(CH₂)₂—,—CH₂O—, —OCH₂—, —CH═CH— or —(CH₂)₄—, the viscosity of the compound canbe relatively small. In the case where Z¹¹, Z¹², Z² and Z³ are a singlebond, —(CH₂)₂— or —CH═CH—, the viscosity of the compound can be furthersmall.

In the case where Z¹¹, Z¹², Z² and Z³ include —CH═CH—, the temperaturerange of the liquid crystal phase can be enhanced, the elastic constantratio K₃₃/K₁₁ can be large, and the viscosity of the compound can besmall. The addition of the liquid crystal compound to a liquid crystalcomposition increases the maximum temperature (T_(NI)) of a nematicphase.

In the case where Z¹¹, Z¹², Z² and Z³ are a single bond, the elasticconstant K₃₃ can be small.

One of X₁ and X₂ is fluorine, and the other thereof is chlorine, i.e.,X₁ and X₂ are different halogens. In the case where one of X₁ and X₂ isfluorine with the other thereof being chlorine, the compatibility withother liquid crystal compounds can be improved in comparison to the casewhere both X₁ and X₂ are fluorine. Accordingly, the liquid crystalcompound (1) can be added in a larger amount than the other liquidcrystal compounds, whereby a liquid crystal composition having a higherdielectric anisotropy (Δ∈) than the conventional liquid crystalcomposition can be obtained, and the temperature range where the liquidcrystal composition can be used as a liquid crystal device can beenhanced.

Furthermore, in the case where X₁ is chlorine, and X₂ is fluorine, thecompatibility with other liquid crystal compounds is further improved,and the compounds represented by formulas (b) and (d) are particularlyexcellent in compatibility.

In the case where:

in formula (a), rings B and C are trans-1,4-cyclohexylene, and Z² and Z³are a single bond,

in formula (b), rings A¹ and B are trans-1,4-cyclohexylene, Z¹¹ is asingle bond, and Z² is —CH₂O—, and

in formula (d), rings A¹, A² and B are trans-1,4-cyclohexylene, Z¹¹ andZ¹² are a single bond, and Z² is a single bond or —CH₂O—,

Rb is one of linear alkoxy having 1 to 9 carbons, linear alkoxyalkylhaving 2 to 9 carbons, linear alkenyl having 2 to 10 carbons, linearalkenyloxy having 2 to 9 carbons, linear fluoroalkyl having 1 to 10carbons, and linear fluoroalkoxy having 1 to 9 carbons.

The liquid crystal compound (1) may contain such an amount of anisotope, such as ²H (deuterium) and ¹³C, that is larger than the naturalabundance because the presence of an isotope causes no large differencein characteristics of the compound.

In the case where the liquid crystal compound (1) has three rings havinga 1,4-phenylene skeleton and/or a trans-1,4-cyclohexylene skeleton, theviscosity can be small, and the maximum temperature of a nematic phasecan be increased.

In the case where the liquid crystal compound (1) has four of theaforementioned rings, the maximum temperature of a nematic phase can befurther increased.

The liquid crystal compound (1) can be adjusted to have desiredcharacteristics including the optical anisotropy (Δn) and the dielectricanisotropy (Δ∈) by suitably selecting the end groups Ra and Rb, therings A¹, A³, B and C, and the bonding groups Z¹¹, Z¹², Z² and Z³ withinthe aforementioned ranges.

(Preferred Embodiments of Liquid Crystal Compound (1))

In the liquid crystal compound (1), compounds represented by formulas(a-1) to (d-1) are preferred. The compounds represented by formulas(a-1) to (d-1) can enhance the temperature range of the liquid crystalphase, can decrease the viscosity, can increase the optical anisotropy(Δn), and can negatively increase the dielectric anisotropy (Δ∈).

In the formulas (a-1) to (d-1), Ra₁ and Rb₁ are independently linearalkyl having 1 to 10 carbons, provided that in the alkyl, —CH₂— may bereplaced by —O—, —(CH₂)₂— may be replaced by —CH═CH—, and hydrogen maybe replaced by a halogen.

Rings A¹, A² and B, the bonding groups Z¹¹, Z¹² and Z³, and the groupsX₁ and X₂ are the same as in the liquid crystal compound (1).

In the case where:

in formula (b-1), rings A¹ and B are trans-1,4-cyclohexylene, Z¹¹ is asingle bond, and Z² is —CH₂O—, and

in formula (d-1), rings A¹, A² and B are trans-1,4-cyclohexylene, Z¹¹and Z¹² are a single bond, and Z² is a single bond or —CH₂O—,

Rb₁ is one of linear alkoxy having 1 to 9 carbons, linear alkoxyalkylhaving 2 to 9 carbons, linear alkenyl having 2 to 10 carbons, linearalkenyloxy having 2 to 9 carbons, linear fluoroalkyl having 1 to 10carbons, and linear fluoroalkoxy having 1 to 9 carbons.

Among the compounds represented by formulas (a-1) to (d-1), such acompound is preferred that Ra₁ and Rb₁ are independently linear alkylhaving 1 to 10 carbons, linear alkoxy having 1 to 9 carbons, linearalkoxyalkyl having 1 to 9 carbons, linear alkenyl having 2 to 10carbons, linear alkenyloxy having 2 to 9 carbons, linear fluoroalkylhaving 1 to 10 carbons or linear fluoroalkoxy having 1 to 9 carbons, andZ¹¹, Z¹², Z² and Z³ are independently a single bond, —(CH₂)₂—, —CH═CH—,—CH₂O— or —OCH₂—.

In the preferred compound, it is preferred that Ra₁ is linear alkylhaving 1 to 10 carbons or linear alkenyl having 2 to 10 carbons,

Rb₁ is linear alkyl having 1 to 10 carbons or linear alkoxy having 1 to9 carbons, and

Z¹¹, Z¹², Z² and Z³ are independently a single bond, —(CH₂)₂—, —CH═CH—,—CH₂O— or —OCH₂—.

It is also preferred that Z¹¹, Z¹², Z² and Z³ are independently a singlebond, —(CH₂)₂— or —CH═CH—. In the case where the compounds (a-1) to(d-1) have the aforementioned structure, the liquid crystal compound canfurther decrease the viscosity and can have excellent compatibility withother liquid crystal compounds, and the addition of the compound to aliquid crystal composition increases a maximum temperature (TNI) of anematic phase.

It is also preferred that Ra₁ is linear alkyl having 1 to 10 carbons orlinear alkenyl having 2 to 10 carbons, Rb₁ is linear alkoxy having 1 to9 carbons, and Z² is —CH₂O—. In the case where the compounds (a-1) to(d-1) have the aforementioned structure, the dielectric anisotropy canbe further negatively increased.

(Preferred Embodiments of Liquid Crystal Compound (b))

In the liquid crystal compound (1) represented by formula (b), preferredexamples of the liquid crystal compound include liquid crystal compoundsrepresented by formulas (b-2-1) to (b-7-1) and (b-2-2) to (b-7-2).

The liquid crystal compounds are particularly excellent in compatibilitywith other liquid crystal compounds.

In the liquid crystal compound represented by formula (b), preferredexamples of the liquid crystal compound also include liquid crystalcompounds represented by formulas (b-8-1) to (b-10-1) and (b-8-2) to(b-10-2).

The liquid crystal compounds are particularly excellent in compatibilitywith other liquid crystal compounds, and can negatively increase thedielectric anisotropy. In particular, the compound where Rb₃ is linearalkoxy can further negatively increase the dielectric anisotropy.

In the case where the liquid crystal compound has the structurerepresented by formula (1), the compound has suitable negativedielectric anisotropy and is considerably excellent in compatibilitywith other liquid crystal compounds. Furthermore, the compound hasstability to heat, light and so forth, has a nematic phase in a widetemperature range, has small viscosity, suitable optical anisotropy, andsuitable elastic constants K₃₃ and K₁₁. A liquid crystal compositioncontaining the liquid crystal compound (1) is stable under theconditions where a liquid crystal display device is generally used, andsuffers no deposition of the compound as crystals (or a smectic phase)upon storing at a low temperature.

Accordingly, the liquid crystal compound (1) can be favorably applied toa liquid crystal composition used in a liquid crystal display devicehaving such an operation mode as a PC mode, a TN mode, aSTN mode, an ECBmode, an OCB mode, an IPS mode, a VA mode and so forth, and inparticular, can be favorably applied to a liquid crystal compositionused in a liquid crystal display device having an IPS mode or a VA mode.

(Synthesis of Liquid Crystal Compound (1))

The liquid crystal compound (1) can be synthesized by suitably combiningsynthetic methods of organic synthesis chemistry. A method forintroducing the target end groups, rings and bonding groups to astarting material is disclosed, for example, in known publications, suchas Organic Synthesis, published by John Wiley & Sons, Inc., OrganicReactions, published by John Wiley & Sons, Inc., Comprehensive OrganicSynthesis, published by Pergamon Press, and Shin Jikken Kagaku Koza(Lectures on New Experimental Chemistry), published by Maruzen, Inc.

(Formation of Bonding Group Z¹¹, Z¹², Z² or Z³)

An example of the method for forming the bonding group Z¹¹, Z¹², Z² orZ³ will be described. A reaction scheme for forming the bonding group isshown. In the scheme, MSG¹ and MSG² are a monovalent organic group. Theplural groups represented by MSG¹ (or MSG 2) used in the scheme may bethe same as or different from each other. The compounds (1A) to (1G)correspond to the compound (1).

(I) Formation of Double Bond 1

An organic halide (a1) having a monovalent organic group MSG² is reactedwith magnesium to prepare a Grignard reagent. The Grignard reagent thusprepared is reacted with an aldehyde derivative (a4) or (a5) tosynthesize a corresponding alcohol derivative. Subsequently, theresulting alcohol derivative is subjected to a dehydration reaction byusing an acidic catalyst, such as p-toluenesulfonic acid, to synthesizea corresponding compound (1A) or (1B) having a double bond.

(II) Formation of Double Bond 2

A compound obtained by treating an organic halide (a1) with butyllithiumor magnesium is reacted with a formamide, such as N,N-dimethylformamide(DMF), to obtain an aldehyde (a6). The resulting aldehyde (a6) isreacted with a phosphoylide obtained by treating a phosphonium salt (a7)or (a8) with a base, such as potassium t-butoxide, to synthesize acorresponding compound (1A) or (1B) having a double bond. In thereaction, a cis compound may be formed depending on the reactionconditions, and in the case where a trans compound is necessarilyobtained, the cis compound is isomerized to the trans compound by aknown method.

(III) Formation of Single Bond 1

An organic halide (a1) is reacted with magnesium to prepare a Grignardreagent. The Grignard reagent thus prepared is reacted with acyclohexanone derivative (a2) to synthesize a corresponding alcoholderivative. Subsequently, the resulting alcohol derivative is subjectedto a dehydration reaction by using an acidic catalyst, such asp-toluenesulfonic acid, to synthesize a corresponding compound (a3)having a double bond. The resulting compound (a3) is hydrogenated in thepresence of a catalyst, such as Raney-Ni, to synthesize a compound (1C).The cyclohexanone derivative (a2) can be synthesized, for example, bythe method disclosed in JP S59-7122 A/1984.

(IV) Formation of Single Bond 2

A dihydroxyborane derivative (a9) and an organic halide (a1) are reactedin the presence, for example, of a catalyst containing a carbonateaqueous solution and tetrakis(triphenylphosphine)palladium (Pd(PPh₃)₄)to synthesize a compound (1F).

In alternative, an organic halide (a10) having a monovalent organicgroup MSG¹ is reacted with butyllithium and then reacted with zincchloride, and thereafter, the resulting compound is reacted with acompound (a1) in the presence, for example, ofbistriphenylphosphinedichloropalladium (Pd(PPh₃)₂Cl₂) to synthesize acompound (1F)

(V) Formation of —(CH₂)₂—

A compound (1A) is hydrogenated in the presence of a catalyst, such ascarbon-supported palladium (Pd/C) to synthesize a compound (1D).

(VI) Formation of —(CH₂)₄—

A compound (1B) is hydrogenated in the presence of a catalyst, such ascarbon-supported palladium (Pd/C) to synthesize a compound (1E).

(VII) Formation of —CH₂O— or —OCH₂—

A dihydroxyborane derivative (a11) is oxidized with an oxidizing agent,such as hydrogen peroxide, to obtain an alcohol derivative (a12).Separately, an aldehyde derivative (a6) is reduced with a reducingagent, such as sodium borohydride, to obtain a compound (a13). Theresulting compound (a13) is halogenated, for example, with hydrobromicacid to obtain an organic halide (a14). The compound (a12) and thecompound (a14) thus obtained are reacted in the presence, for example,of potassium carbonate to synthesize a compound (1G).

(Production Method of Compounds (I) and (II))

An example of the production method of compounds (I) and (II), which maybe a starting material of the liquid crystal compound (1), will bedescribed.

An aniline derivative (b1) is reacted with sodium nitrite and a mineralacid under cooling with ice to obtain a diazonium salt. The resultingdiazonium salt is reacted with hydrochloric acid and cuprous chlorideand then subjected to steam distillation to obtain a compound (b2). Theresulting compound (b2) is etherified by reacting with an alcoholderivative (R′OH) in the presence of a base, such as potassiumhydroxide, to obtain a compound (b3). The resulting compound (b3) isreacted with a halogen molecule, such as bromine and iodine, to producea compound (I′) as an example of the compound (I) of the invention.

An aniline derivative (b4) is reacted with sodium nitrite and a mineralacid under cooling with ice to obtain a diazonium salt. The resultingdiazonium salt is boiled in water. According to the operation, adecomposition reaction occurs to obtain a phenol derivative (b5), inwhich the amino group in (b4) converted into hydroxyl group. Theresulting compound (b5) is etherified by reacting with a correspondingorganic halide (R′—X) in the presence of a base, such as potassiumhydroxide, to obtain a compound (b6). The resulting compound (b6) isreacted with a halogen molecule, such as bromine and iodine, to producea compound (II′) as an example of the compound (II) of the invention.

(Production Method of Liquid Crystal Compound (1))

Examples of the production method of the liquid crystal compound (1),i.e., the liquid crystal compound represented by formulas (a) to (d),will be described.

A compound (b7) is reacted with magnesium to prepare a Grignard reagent.The Grignard reagent is reacted with a carbonyl derivative (b8) toobtain an alcohol derivative (b9). The resulting alcohol derivative (b9)is subjected to a dehydration reaction in the presence of an acidiccatalyst, such as p-toluenesulfonic acid (PTS), to obtain a compound(b10). The compound (b10) is then subjected to a hydrogenation reactionin the presence of a catalyst, such as Pd/C or Raney-Ni, to obtain acompound (b11) as an example of the liquid crystal compound (1) of theinvention.

A compound (b7) is reacted with magnesium to prepare a Grignard reagent.The Grignard reagent is reacted with a boronic acid ester and hydrolyzedin an acidic atmosphere to obtain a dihydroxyborane derivative (b12).The dehydroxyboran derivative (b12) and a compound (b13) are reacted inthe presence of a base, such as potassium carbonate or sodium hydroxide,and a catalyst, such as Pd/C, Pd(PPh₃)₄ or Pd(PPh₃)₂Cl₂, to obtain acompound (b14) as an example of the liquid crystal compound (1) of theinvention.

A compound (b7) is reacted with magnesium to prepare a Grignard reagent.The Grignard reagent is reacted with N,N-dimethylformamide andhydrolyzed in an acidic atmosphere to obtain an aldehyde derivative(b15). The resulting aldehyde derivative (b15) is reduced, for example,with sodium borohydride and then chlorinated, for example, with thionylchloride, and is then further subjected to an Arbusov reaction withtriethyl phosphite to obtain a compound (b18). The compound (b18) and analdehyde derivative (b19) are reacted in the presence of a base, such assodium ethoxide. Depending on necessity, isomers thus formed (E compoundor Z compound) are isomerized, for example, with benzenesulfinic acid toproduce a compound (b20) as an example of the liquid crystal compound(1) of the invention.

A compound (b7) is reacted with magnesium to prepare a Grignard reagent.The Grignard reagent is reacted with a carbonyl derivative (b21) toobtain an alcohol derivative (b22). The resulting alcohol derivative(b22) is subjected to dehydration reaction in the presence of an acidiccatalyst, such as p-toluenesulfonic acid, to obtain a compound (b23).The compound (b23) is subjected to a hydrogenation reaction in thepresence of a catalyst, such as Pd/C, to obtain a compound (b24). Thecompound (b24) is hydrolyzed in an acidic atmosphere, such as formicacid, to obtain a carbonyl derivative (b25). The resulting carbonylderivative (b25) is subjected to Wittig reaction with a phosphoylideprepared from methoxymethyltriphenylphosphonium chloride and a base,such as potassium t-butoxide (t-BuOK), to obtain an enol etherderivative (b26). The resulting enol ether derivative (b26) ishydrolyzed in an acidic atmosphere, and then is isomerized in a basicatmosphere depending on necessity, to obtain an aldehyde derivative(b27). The aldehyde derivative (b27) is reacted with a phosphoylideprepared from methyltriphenylphosphonium bromide and a base, such ast-BuOK, to obtain a compound (b28) as an example of the liquid crystalcompound (1) of the invention.

A compound (b19) is reduced, for example, with sodium borohydride toobtain a compound (b29). Subsequently, the compound (b29) is brominated,for example, with hydrobromic acid to obtain a compound (b30).Separately, a dihydroxyborane derivative (b12) is subjected to anoxidation reaction with an oxidizing agent, such as hydrogen peroxide,to obtain a phenol derivative (b31). The compound (b30) and the phenolderivative (b31) obtained by the aforementioned operations are subjectedto an etherification reaction in the presence of a base, such aspotassium carbonate, to obtain a compound (b32) as an example of theliquid crystal compound (1) of the invention.

A compound (b33) is reacted with magnesium to prepare a Grignardreagent. The Grignard reagent is reacted with a carbonyl derivative(b34) to obtain an alcohol derivative (b35). The resulting alcoholderivative (b35) is subjected to a dehydration reaction in the presenceof an acidic catalyst, such as p-toluenesulfonic acid, to obtain acompound (b36). The compound (b36) is subjected to a hydrogenationreaction in the presence of a catalyst, such as Raney-Ni, to obtain acompound (b37). The compound (b37) is then subjected to a demethylationreaction with a Lewis acid, such as boron tribromide, to obtain a phenolderivative (b38). The resulting phenol derivative (b38) is subjected toan etherification reaction with a compound (b39) in the presence of abase, such as potassium carbonate, to obtain a compound (b40) as anexample of the liquid crystal compound (1) of the invention.

A compound (b38) is reacted with trifluoromethanesulfonic anhydride inthe presence of a base, such as pyridine, to obtain a compound (b41).Subsequently, the compound (b41) is reacted with a dihydroxyboranederivative (b42) in the presence of a base, such as potassium carbonate,with Pd(PPh₃)₄ or Pd/C as a catalyst to obtain a compound (b43) as anexample of the liquid crystal compound (1) of the invention.

(Liquid Crystal Composition)

The liquid crystal composition of the invention will be described. Thecomponents of the liquid crystal composition contain at least one of theliquid crystal compound (1), and may contain two or more liquid crystalcompounds (1) or may be constituted only by the liquid crystal compound(1). The content of the liquid crystal compound (1) in the liquidcrystal composition of the invention is not particularly limited, and itis preferred that approximately 1 to approximately 99% by weight of theliquid crystal compound (1) is contained based on the total weight ofthe liquid crystal composition. Upon preparing the liquid crystalcomposition of the invention, the components may be selected inconsideration, for example, of the dielectric anisotropy of the liquidcrystal compound (1).

(Liquid Crystal Display Device)

The liquid crystal composition of the invention can be applied to aliquid crystal display device having such an operation mode as a PCmode, a TN mode, a STN mode, a BTN mode, an ECB mode, an OCB mode, anIPS mode, a VA mode and so forth, and in particular, can be favorablyapplied to a liquid crystal display device having an IPS mode or a VAmode utilizing vertical orientation. The driving mode of the liquidcrystal display device may be a passive packing (PM) or an activepacking (AM).

The liquid crystal display device of the invention can be used as anematic curvilinear aligned phase (NCAP) device prepared bymicrocapsulating the liquid crystal composition, and a polymer dispersed(PD) device having a three dimensional net-work polymer formed in theliquid crystal composition, for example, a polymer network (PN) device.

EXAMPLE

The invention will be described in more detail with reference toexamples, but the invention is not construed as being limited to theexamples. All “%” means “% by weight” unless otherwise indicated.

The resulting compounds are identified by a nuclear magnetic resonancespectrum obtained by ¹H-NMR analysis, a gas chromatogram obtained by gaschromatography (GC), and so forth, and the analysis methods aredescribed below.

¹H-NMR Analysis

DRX-500 (produced by Bruker Biospin Co. Ltd.) was used as a measuringequipment. The measurement was carried out by dissolving a sampleproduced in the example in a deuterated solvent, such as CDCl₃, underconditions of room temperature, 500 MHz and an accumulation number of24. In the description of the resulting nuclear magnetic resonancespectrum, “s” means a singlet, “d” means a doublet, “t” means a triplet,“q” means a quartet, and “m” means a multiplet. Tetramethylsilane (TMS)was used as a standard substance for the zero point of chemical shift δ.

GC Analysis

Gas chromatograph Model GC-14B, produced by Shimadzu Corp. was used as ameasuring equipment. A capillary column CBP1-M25-025 (length: 25 m,bore: 0.22 mm, film thickness: 0.25 μm, fixed liquid phase:dimethylpolysiloxane, non-polar), produced by Shimadzu Corp. was used asa column. Helium was used as a carrier gas with a flow rate adjusted to1 mL/min. The temperature of the sample vaporizing chamber was adjustedto 280° C., and the temperature of the detector (FID) was adjusted to300° C.

The sample was dissolved in toluene to prepare a solution having aconcentration of 1% by weight, and 1 μL of the resulting solution wasinjected to the sample vaporizing chamber.

The recorder used was Chromatopac Model C—R6A, produced by ShimadzuCorp. or its equivalent. A gas chromatogram obtained showed a retentiontime of a peak and a peak area corresponding to the component compound.

Solvents for diluting the sample may also be chloroform, hexane, and soforth. The following capillary columns may also be used: DB-1 made byAgilent Technologies Inc. (length 30 m, bore 0.32 mm, film thickness0.25 μm), HP-1 made by Agilent Technologies Inc. (length 30 m, bore 0.32mm, film thickness 0.25 μm), Rtx-1 made by Restek Corp. (length 30 m,bore 0.32 mm, film thickness 0.25 μm), and BP-1 made by SGEInternational Pty. Ltd. (length 30 m, bore 0.32 mm, film thickness 0.25μm).

An area ratio of each peak in the gas chromatogram corresponds to aratio of the component compound. Percentage by weight of the componentcompound is not completely identical to an area ratio of each peak. Inthe case where the aforementioned columns are used in the invention,however, the percentage by weight of the component compoundsubstantially corresponds to the percentage of the area of each peak ofthe sample analyzed because the correction coefficient issubstantially 1. This is because there is no significant difference incorrection efficient of component compounds. In order to obtain moreprecisely the compositional ratio of the liquid crystal compounds in theliquid crystal composition by gas chromatogram, an internal referencemethod is applied to gas chromatogram. The liquid crystal compoundcomponents (components to be measured) having been precisely weighed anda standard liquid crystal compound (standard substance) aresimultaneously measured by gas chromatography, and the relativeintensity of the area ratio of peaks of the components to be measuredand a peak of the standard substance is calculated in advance. Thecompositional ratio of the liquid crystal compounds in the liquidcrystal composition can be precisely obtained by gas chromatographyanalysis by correcting using the relative intensity of the peak areas ofthe components with respect to the standard substance.

(Measurement Sample of Characteristics of Liquid Crystal Compounds andso Forth)

A sample to be measured for characteristics of the liquid crystalcompound includes two cases, i.e., a compound itself is used as asample, and a compound is mixed with base mixture to prepare a sample.

In the later case where a sample obtained by mixing a compound with basemixture is used, the measurement is carried out in the following manner.A sample for measurement was prepared by mixing 15% by weight of theresulting liquid crystal compound and 85% by weight of base mixture.Characteristics of the compound were calculated by extrapolating from avalue obtained by the measurement according to the following equation.extrapolated value=(100×(measured value of sample)−(weight % of basemixture)×(measured value of mother crystals))/(weight % of liquidcrystal compound)

When a smectic phase or crystals are separated out at this ratio at 25°C., a ratio of the compound and base mixture was changed step by step inthe order of (10% by weight/90% by weight), (5% by weight/95% byweight), (1% by weight/99% by weight), respectively. A sample having nosmectic phase or crystal separated out at 25° C. was measured forcharacteristics, and an extrapolated value was obtained according to theaforementioned equation, which is designated as characteristics of theliquid crystal compound.

While there were various kinds of base mixture used in the measurement,the base mixture A, for example, has the following composition.

Base Mixture A:

As a sample for measuring characteristics of a liquid crystalcomposition, a liquid crystal composition itself was used.

(Measuring Method of Characteristics of Liquid Crystal Compounds and soForth)

Measurement of the characteristics was carried out according to thefollowing methods. Most methods are described in the Standard ofElectric Industries Association of Japan, EIAJ ED-2521 A or those withsome modifications. A TFT was not attached to a TN device used formeasurement.

Among the measured values, values obtained with the liquid crystalcompound itself as a sample and values obtained with the liquid crystalcomposition itself as a sample are indicated as experimental data asthey are. In the case of values obtained with samples obtained by mixinga compound with base mixture, values obtained by the extrapolatingmethod is indicated as extrapolated values.

Phase Structure and Phase Transition Temperature (° C.)

The measurement was carried out by the following methods (1) and (2).

(1) A compound was placed on a hot plate (Hot Stage Model FP-52,produced by Mettler Co., Ltd.) of a melting point measuring apparatusequipped with a polarizing microscope, and while the compound was heatedat a rate of 3° C. per minute, the phase state and changes thereof wereobserved with the polarizing microscope to determine the kind of phase.

(2) A compound was increased and decreased in temperature at a rate of3° C. per minute by using a scanning calorimeter DSC-7 System or DiamondDSC System, produced by Perkin-Elmer, Inc., and starting points of anendothermic peak and an exothermic peak associated with phase change ofthe sample were obtained by extrapolation (on set) to determine thephase change temperature.

In the following, crystals are shown by “C”. In the case where crystalsare distinguished, they are shown by “C₁” or “C₂”. A smectic phase isshown by “S”, and a nematic phase is shown by “N”. A liquid (isotropic)is shown by “Iso”. In the case where a smectic B phase and a smectic Aphase are distinguished from each other in the smectic phase, they areshown by “S_(B)” and “S_(A)”, respectively. The transition temperaturesare shown, for example, by “C 50.0 N 100.0 Iso”, which means that thetransition temperature from crystals to a nematic phase (CN) is 50.0°C., and the transition temperature from a nematic phase to a liquid (NI)is 100.0° C. This rule is applied to the other expressions.

Maximum Temperature of Nematic Phase (T_(NI); ° C.)

A sample was placed on a hot plate (Hot Stage Model FP-52, produced byMettler Co., Ltd.) in a melting point measuring apparatus equipped witha polarizing microscope, and while the compound was heated at a rate of1° C. per minute, the phase state and changes thereof were observed withthe polarizing microscope. A temperature was measured when a part of thesample began to change from a nematic phase into an isotropic liquid. Ahigher limit of a temperature range of a nematic phase may beabbreviated to “a maximum temperature”.

Low Temperature Compatibility

Samples were prepared by mixing base mixture and a liquid crystalcompound to provide an amount of the liquid crystal compound of 20% byweight, 15% by weight, 10% by weight, 5% by weight, 3% by weight and 1%by weight, and the samples were placed in glass bottles. The glassbottles were stored in a freezer at −10° C. or −20° C. for a prescribedperiod of time, and then they were observed as to whether or notcrystals or a smectic phase was deposited.

Viscosity (η; mPa·s, Measured at 20° C.)

A viscosity was measured by means of an E-type viscometer.

Rotation Viscosity (γ1; mPa·s, Measured at 25° C.)

A rotation viscosity was measured according to the method disclosed inM. Imai, et al., Molecular Crystals and Liquid Crystals, vol. 259, p. 37(1995). A sample was placed in a VA device having a distance between twoglass plates (cell gap) of 20 μm. The device was applied with a voltagein a range of from 30 V to 50 V stepwise by 1 V. After a period of 0.2second with no application of voltage, voltage application was repeatedwith only one rectangular wave (rectangular pulse of 0.2 second) andapplication of no voltage (2 seconds). A peak current and a peak time ofa transient current that was generated by the application of voltagewere measured. A value of rotation viscosity was obtained from themeasured values and the calculating formula (8) in the literature by M.Imai, et al. The value of dielectric anisotropy, which was necessary forthe calculation, was obtained according to the following measuringmethod of dielectric anisotropy.

Optical Anisotropy (Δn; Measured at 25° C.)

Measurement was carried out with an Abbe refractometer mounting apolarizing plate on an ocular using a light at a wavelength of 589 nm ata temperature of 25° C. The surface of a main prism was rubbed in onedirection, and then a sample (a liquid crystal composition or a mixtureof a liquid crystal compound and base mixture) was dropped on the mainprism. Refractive index (n∥) was measured when the direction of apolarized light was parallel to that of the rubbing. Refractive index(n⊥) was measured when the direction of a polarized light wasperpendicular to that of the rubbing. A value of optical anisotropy wascalculated from the equation;Δn=n∥−n⊥.Dielectric Anisotropy (Δ∈; Measured at 25° C.)

Dielectric anisotropy was measured in the following manner.

An ethanol solution (20 mL) of octadecyltriethoxysilane (0.16 mL) wascoated on a glass plate having been well washed. The glass plate wasrotated with a spinner and then heated to 150° C. for 1 hour. A VAdevice having a distance (cell gap) of 20 μm was fabricated with twoglass plates.

A polyimide alignment film was prepared on a glass plate in the samemanner. After rubbing the alignment film formed on the glass plate, a TNdevice having a distance between two glass plates of 9 μm and a twistedangle of 80° was fabricated.

A sample (a liquid crystal composition or a mixture of a liquid crystalcompound and base mixture) was poured into the resulting VA device, anda voltage of 0.5 V (1 kHz, sine waves) was applied thereto to measure adielectric constant (∈∥) in parallel to a major axis of liquid crystalmolecules.

A sample (a liquid crystal composition or a mixture of a liquid crystalcompound and base mixture) was poured into the resulting TN device, anda voltage of 0.5 V (1 kHz, sine waves) was applied thereto to measure adielectric constant (∈⊥) in parallel to a major axis of liquid crystalmolecules.

A value of dielectric anisotropy was calculated from the equation;Δ∈=∈∥−∈⊥.

Voltage Holding Ratio (VHR; Measured at 25° C.; %)

A TN device used for measurement has a polyimide alignment film, and thecell gap between two glass plates is 6 μm. A sample (a liquid crystalcomposition or a mixture of a liquid crystal compound and base mixture)was poured into the device, and then the device was sealed by anadhesive which polymerized by the irradiation of ultraviolet light. TheTN device was impressed and charged with pulse voltage (60 microsecondsat 5 V). Decreasing voltage was measured for 16.7 milliseconds with HighSpeed Voltmeter and the area A between a voltage curve and a horizontalaxis in a unit cycle was obtained. The area B was an area withoutdecreasing. Voltage holding ratio is a percentage of the area A to thearea B.

Examples of intermediate compounds (I) and (II) useful for producing theliquid crystal compound (1) of the invention will be described.

Example 1 Synthesis of 1-bromo-3-chloro-4-ethoxy-2-fluorobenzene (C2)

First Step

550 g of hydrochloric acid was added to a reactor having 270 g of waterplaced therein, and 129 g of 2,6-difluoroaniline (b1) was further addedthereto, followed by stirring for 30 minutes at 60° C. Thereafter, themixture was cooled to −10° C., and 192.5 g of a 37.6% sodium nitriteaqueous solution was added dropwise thereto over 30 minutes in atemperature range of −10 to −5° C., followed by stirring for 30 minutesat −10° C. The resulting reaction mixture was added to another reactorhaving 122 g of 30% hydrochloric acid and 22 g of cuprous chlorideplaced therein over 90 minutes in a temperature range of 25 to 30° C.,followed by stirring for 30 minutes in that temperature range. Areaction mixture obtained by the reaction was subjected to steamdistillation. The resulting organic phase was washed with water in threetimes and then dried to obtain 124 g of 2-chloro-1,3-difluorobenzene(b2).

Second Step

560 g of potassium hydroxide and 23 g of tetramethylammonium chloride(TMAC) were added to a reactor having 2,000 mL of ethanol placed thereinin a temperature range of 50 to 60° C., followed by stirring for 30minutes in that temperature range. Thereafter, the solution was heatedto 80° C., and 594 g of a compound (b2) was added thereto over 1 hour ina temperature range of 80 to 85° C., followed by stirring for 5 hours at80° C. After cooling the resulting reaction mixture to 25° C., 1,000 mLof toluene and 500 mL of water were added thereto and well mixed, andthe mixture was left at rest to separate into an organic layer and anaqueous layer. After collecting the resulting organic layer, 500 mL oftoluene was newly added to the aqueous mixture and well mixed, and themixture was subjected to the same operation to extract again thecompound contained in the aqueous layer. The toluene solution was addedto the organic layer. After washing the organic layer with water inthree times, the resulting organic layer was distilled under reducedpressure to obtain 606 g of 2-chloro-1-ethoxy-3-fluorobenzene (b43). Theresulting liquid was colorless and had a boiling point of 98 to 99° C./8mmHg.

Third Step

606 g of the compound (b43) was added to a reactor in a nitrogenatmosphere, to which 570 g of bromine was added dropwise over 1 hour ina temperature range of 20 to 40° C., followed by stirring for 30minutes. The resulting reaction mixture was washed with a saturatedsodium thiosulfate aqueous solution, a 10% sodium hydroxide aqueoussolution, and water. The resulting reaction mixture having been washedwas subjected to fractional distillation under reduced pressure toobtain 760 g of 1-bromo-3-chloro-4-ethoxy-2-fluorobenzene (C2). Theresulting compound (C2) was white solid and had a melting point of 65.4to 66.1° C. and a boiling point of 125 to 127° C./8 mmHg.

The resulting compound exhibited the following chemical shift δ (ppm) of¹H-NMR analysis, and thus the compound was identified as1-bromo-3-chloro-4-ethoxy-2-fluorobenzene. The measuring solvent wasCDCl₃.

Chemical shift δ(ppm): 7.35 (t, 1H), 6.62 (dd, 1H), 4.09 (q, 2H), 1.48(t, 3H)

Example 2 Synthesis of 1-bromo-2-chloro-4-ethoxy-3-fluorobenzene (C12)

First Step

728 g of 3-chloro-2-fluoroaniline was added to a reactor having 6,860 gof 30.6% sulfuric acid placed therein, followed by stirring for 30minutes at 80° C. Thereafter, the mixture was cooled to −10° C., and 952g of a 37.0% sodium nitrite aqueous solution was added dropwise theretoover 90 minutes in a temperature range of −10 to −5° C., followed bystirring for 30 minutes in that temperature range. The resultingreaction mixture was added to another reactor having 4,100 g of 51.2%sulfuric acid, 1,500 g of copper sulfate and 3,000 mL of toluene placedtherein over 6 hours in a temperature range of 80 to 85° C., followed bystirring for 30 minutes in that temperature range. The resultingreaction mixture was cooled to a temperature range of 70 to 75° C. andleft at rest to separate into two layers, i.e., an organic layer and anaqueous layer, and the organic layer was collected. The aqueous layerwas cooled to 20° C., and copper sulfate was filtered off, followed byextracting with 1,200 mL toluene twice. The organic layer obtained byextraction was washed with 700 mL of water and subjected to fractionaldistillation to obtain 300 g of 3-chloro-2-fluorophenol (b5). Thecompound had a boiling point of 60 to 62° C./1 mmHg.

Second Step

The compound (b5) was added dropwise to a reactor having 1,200 g of a10% sodium hydroxide aqueous solution placed therein over 30 minutes ina temperature range of 20 to 40° C. Thereafter, 462 g of diethyl sulfatewas added dropwise thereto over 1 hour in a temperature range of 25 to35° C., followed by stirring for 5 hours in that temperature range. Theresulting organic layer was collected and washed with 200 mL of water inthree times, followed by drying, to obtain 505 g of1-chloro-3-ethoxy-2-fluorobenzene (b44). The resulting liquid wascolorless.

Third Step

504 g of the compound (b44) was added to a reactor in a nitrogenatmosphere, to which 434 g of bromine was added dropwise over 1 hour ina temperature range of 20 to 40° C., followed by stirring for 30minutes. The resulting reaction mixture was washed with a saturatedsodium thiosulfate aqueous solution, a 10% sodium hydroxide aqueoussolution, and water. The residue was subjected to fractionaldistillation under reduced pressure to obtain 605 g of1-bromo-2-chloro-4-ethoxy-3-fluorobenzene (C12). The resulting compound(C12) was white solid and had a melting point of 48.0 to 48.5° C. and aboiling point of 88 to 90° C./1 mmHg.

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified as1-bromo-2-chloro-4-ethoxy-3-fluorobenzene. The measuring solvent wasCDCl₃.

Chemical shift δ(ppm): 7.31 (dd, 1H), 6.77 (t, 1H), 4.09 (q, 2H), 1.45(t, 3H)

Example 3

The following compounds (C1), (C3) to (C11) and (C13) to (C20) weresynthesized in the same method as the synthesis methods described inExamples 1 and 2. The compounds (C2) and (C12) obtained in Examples 1and 2 are also described in the following. The values shown with thecompounds are values measured in the aforementioned methods, in which“m.p.” shows a melting point, and “b.p.” shows a boiling point.

Examples of the liquid crystal compound (1) of the invention produced byusing the compounds (C1) to (C20) synthesized in Examples 1, 2 and 3will be described.

Example 4 Synthesis oftrans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4-propyl-bicyclohexyl(C28)

First Step

2.6 g of well dried magnesium and 20 mL of THF were added to a reactorin a nitrogen atmosphere and heated to 40° C. 26.6 g of the compound(C2) dissolved in 80 mL of THF was added dropwise thereto slowly in atemperature range of 30 to 45° C., followed by stirring for 30 minutes.Thereafter, 22.2 g of 4′-propyl-bicyclohexyl-4-one (b45) dissolved in 40mL of THF was added dropwise thereto slowly in a temperature range of 30to 50° C., followed by stirring for 60 minutes. The resulting reactionmixture was cooled to 25° C. and then poured into 100 mL of 3Nhydrochloric acid and 100 mL of toluene, followed by mixing. The mixturewas then left to rest to separate into an organic layer and an aqueouslayer, followed by extracting. The resulting organic layer was collectedand washed with water, a 2N sodium hydroxide aqueous solution, asaturated sodium hydrogen carbonate aqueous solution and water, followedby drying over anhydrous magnesium sulfate. Thereafter, the solvent wasdistilled off under reduced pressure to obtain 45.8 g of4-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4′-propyl-bicyclohexyl-4-ol(b46). The resulting compound (b46) was a yellow oily substance.

Second Step

45.8 g of the compound (b46), 0.5 g of p-toluenesulfonic acid and 150 mLof toluene were mixed, and the mixture was refluxed under heating for 1hour while removing distilled water. After cooling the reaction mixtureto 25° C., 200 mL of water and 100 mL of toluene was added to theresulting liquid, and the mixture was left at rest to separate into anorganic layer and an aqueous layer, followed by extracting to theorganic layer. The resulting organic layer was collected and washed witha 2N sodium hydroxide aqueous solution, a saturated sodium hydrogencarbonate aqueous solution and water, followed by drying over anhydrousmagnesium sulfate. Thereafter, the solvent was distilled off underreduced pressure to obtain a residue. The residue was purified bypreparative column chromatography using a mixed solvent of heptane andtoluene (heptane/toluene=2/1 by volume) as a developing solvent andsilica gel as a mediator, and further purified by recrystallization froma mixed solvent of heptane and ethanol (heptane/ethanol=2/1 by volume)to obtain 28.5 g of4-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4′-propyl-bicyclohexyl-3-ene(b47). The yield was 68.4% based on the compound (b45).

The transition temperatures of the resulting compound (b47) were asfollows.

Transition temperature: C₁ 65.4 C₂ 81.1 C₃ 88.9 S_(A) 121.5 N 160.2 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified as4-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4′-propyl-bicyclohexyl-3-ene.The measuring solvent was CDCl₃.

Chemical shift δ(ppm): 7.04 (t, 1H), 6.64 (dd, 1H), 5.87 (t, 1H), 4.09(q, 2H), 2.38-0.86 (m, 27H)

Third Step

20.8 g of the compound (b47) was dissolved in a mixed solvent of 80 mLof toluene and 80 mL of isopropyl alcohol, to which 2.0 g of Raney-Niwas added, followed by stirring in a hydrogen atmosphere at roomtemperature until no hydrogen was absorbed. After completing thereaction, Raney-Ni was removed, the solvent was distilled off, and theresidue was purified by a preparative column chromatography using amixed solvent of heptane and toluene (heptane/toluene=4/1 by volume) asa developing solvent and silica gel as a mediator, and further purifiedby recrystallization from a mixed solvent of heptane and ethanol(heptane/ethanol=2/1 by volume) to obtain 13.8 g oftrans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4-propyl-bicyclohexyl(C28). The resulting compound (C28) was colorless crystals, and theyield was 65.8% based on the compound (b47).

The transition temperatures of the resulting compound (C28) were asfollows.

Transition temperature: C 105.5 S_(B) 16.0 N 168.9 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified astrans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4-propyl-bicyclohexyl.The measuring solvent was CDCl₃.

Chemical shift δ(ppm): 7.01 (t, 1H), 6.65 (dd, 1H), 4.08 (q, 2H), 2.72(tt, 1H), 1.88-0.82 (m, 29H)

Example 5 Synthesis oftrans-4′-(2-chloro-4-ethoxy-3-fluorophenyl)-trans-4-propyl-bicyclohexyl(C44)

First Step

2.6 g of well dried magnesium and 20 mL of THF were added to a reactorin a nitrogen atmosphere and heated to 40° C. 26.6 g of the compound(C12) dissolved in 80 mL of THF was added dropwise thereto slowly in atemperature range of 30 to 45° C., followed by stirring for 20 minutes.Thereafter, 21.2 g of a compound (b45) dissolved in 20 mL of THF wasadded dropwise thereto slowly in a temperature range of 30 to 35° C.,followed by stirring for 60 minutes. The resulting reaction mixture wascooled to 25° C. and then poured into 100 mL of 3N hydrochloric acid and100 mL of toluene, followed by mixing. The mixture was then left to restto separate into an organic layer and an aqueous layer, followed byextracting to the organic layer. The resulting organic layer wascollected and washed with water, a 2N sodium hydroxide aqueous solution,a saturated sodium hydrogen carbonate aqueous solution and water,followed by drying over anhydrous magnesium sulfate. Thereafter, thesolvent was distilled off under reduced pressure to obtain 47.0 g of4-(2-chloro-4-ethoxy-3-fluorophenyl)-trans-4′-propyl-bicyclohexyl-4-ol(b48). The resulting compound (b48) was a yellow oily substance.

Second Step

47.0 g of the compound (b48), 1.0 g of p-toluenesulfonic acid and 200 mLof toluene were mixed, and the mixture was refluxed under heating for 1hour while removing distilled water. After cooling the reaction mixtureto 25° C., 200 mL of water and 200 mL of toluene was added to theresulting liquid, and the mixture was left at rest to separate into anorganic layer and an aqueous layer, followed by extracting to theorganic layer. The resulting organic layer was collected and washed witha 2N sodium hydroxide aqueous solution, a saturated sodium hydrogencarbonate aqueous solution and water, followed by drying over anhydrousmagnesium sulfate. Thereafter, the solvent was distilled off underreduced pressure to obtain a residue. The residue was purified by apreparative column chromatography using a mixed solvent of heptane andtoluene (heptane/toluene=4/1 by volume) as a developing solvent andsilica gel as a mediator, and further purified by recrystallization froma mixed solvent of heptane and ethanol (heptane/ethanol=2/1 by volume)to obtain 19.4 g of4-(2-chloro-4-ethoxy-3-fluorophenyl)-trans-4′-propyl-bicyclohexyl-3-ene(b49). The yield was 53.6% based on the compound (b45).

The transition temperatures of the resulting compound (b49) were asfollows.

Transition temperature: C 71.1 N 130.3 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified as4-(2-chloro-4-ethoxy-3-fluorophenyl)-trans-4′-propyl-bicyclohexyl-3-ene.The measuring solvent was CDCl₃.

Chemical shift δ(ppm): 6.85-6.77 (m, 2H), 5.65 (t, 1H), 4.09 (q, 2H),2.36-0.86 (m, 27H)

Third Step

17.0 g of the compound (b49) was dissolved in a mixed solvent of 50 mLof toluene and 100 mL of isopropyl alcohol, to which 1.7 g of Raney-Niwas added, followed by stirring in a hydrogen atmosphere at roomtemperature until no hydrogen was absorbed. After completing thereaction, Raney-Ni was removed, the solvent was distilled off, and theresidue was purified by a preparative column chromatography using amixed solvent of heptane and toluene (heptane/toluene=4/1 by volume) asa developing solvent and silica gel as a mediator, and further purifiedby recrystallization from a mixed solvent of heptane and ethanol(heptane/ethanol=2/1 by volume) to obtain 6.8 g oftrans-4′-(2-chloro-4-ethoxy-3-fluorophenyl)-trans-4-propyl bicyclohexyl(C40). The resulting compound (C40) was colorless crystals, and theyield was 39.6% based on the compound (b49).

The transition temperatures of the resulting compound (C44) were asfollows.

Transition temperature: C 89.9 N 152.9 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified astrans-4′-(2-chloro-4-ethoxy-3-fluorophenyl)-trans-4-propyl-bicyclohexyl.The measuring solvent was CDCl₃.

Chemical shift δ(ppm): 6.92 (dd, 1H), 6.83 (t, 1H), 4.08 (q, 2H), 2.84(tt, 1H), 1.90-0.83 (m, 29H)

Example 6 Synthesis oftrans-4′-(2-(3-chloro-4-ethoxy-2-fluorophenyl)-vinyl)-trans-4-propyl-bicyclohexyl(C58)

First Step

1.92 g of well dried magnesium and 20 mL of THF were added to a reactorin a nitrogen atmosphere and heated to 45° C. 20.0 g of the compound(C2) dissolved in 80 mL of THF was added dropwise thereto over 60minutes in a temperature range of 45 to 55° C., followed by stirring for10 minutes. Thereafter, 18.0 g of(trans-4′-bicyclohexyl-trans-4-yl)-aldehyde (b50) dissolved in 20 mL ofTHF was added dropwise thereto over 60 minutes in a temperature range of50 to 55° C., followed by stirring for 60 minutes. The resultingreaction mixture was cooled to 25° C. and then poured into 100 mL of 3Nhydrochloric acid and 100 mL of toluene, followed by mixing. The mixturewas then left to rest to separate into an organic layer and an aqueouslayer, followed by extracting to the organic layer. The resultingorganic layer was collected and washed with water, a 2N sodium hydroxideaqueous solution, a saturated sodium hydrogen carbonate aqueous solutionand water, followed by drying over anhydrous magnesium sulfate.Thereafter, the solvent was distilled off under reduced pressure toobtain 33.0 g of1-(3-chloro-4-ethoxy-2-fluorophenyl)-2-(trans-4′-propyl-bicyclohexyl-trans-4-yl)-ethanol(b51). The resulting compound (b51) was a yellow oily substance.

Second Step

33.0 g of the compound (b51), 1.0 g of p-toluenesulfonic acid and 150 mLof toluene were mixed, and the mixture was refluxed under heating for 1hour while removing distilled water. After cooling the reaction mixtureto 30° C., 200 mL of water and 100 mL of toluene was added to theresulting liquid, and the mixture was left at rest to separate into anorganic layer and an aqueous layer, followed by extracting to theorganic layer. The resulting organic layer was collected and washed witha 2N sodium hydroxide aqueous solution, a saturated sodium hydrogencarbonate aqueous solution and water, followed by drying over anhydrousmagnesium sulfate. Thereafter, the solvent was distilled off underreduced pressure to obtain a residue. The resulting residue was purifiedby a preparative column chromatography using a mixed solvent of heptaneand toluene (heptane/toluene=4/1 by volume) as a developing solvent andsilica gel as a mediator, and further purified by recrystallization froma mixed solvent of heptane and ethanol (heptane/ethanol=2/1 by volume)to obtain 22.3 g oftrans-4′-(2-(3-chloro-4-ethoxy-2-fluorophenyl)-vinyl)-trans-4-propyl-bicyclohexyl(C58). The resulting compound (C58) was colorless crystals, and theyield was 76.4% based on the compound (b50).

The transition temperatures of the resulting compound (C58) were asfollows.

Transition temperature: C₁ 83.6 C₂ 88.9 S_(A) 125.6 N 224.8 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified astrans-4′-(2-(3-chloro-4-ethoxy-2-fluorophenyl)-vinyl)-trans-4-propyl-bicyclohexyl.The measuring solvent was CDCl₃.

Chemical shift δ(ppm): 7.24 (t, 1H), 6.65 (dd, 1H), 6.39 (d, 1H), 6.11(q, 1H), 4.10 (q, 2H), 2.08-0.81 (m, 30H)

Example 7 Synthesis oftrans-4′-(2-(2-chloro-4-ethoxy-3-fluorophenyl)-ethyl)-trans-4-propyl-bicyclohexyl(C96)

18.0 g oftrans-4′-(2-(2-chloro-4-ethoxy-3-fluorophenyl)-vinyl)-trans-4-propyl-bicyclohexyl(C67) was dissolved in a mixed solvent of 80 mL of toluene and 40 mL ofSolmix A-11 (available from Nippon Alcohol Hanbai K. K.), to which 0.5 gof Pd/C was further added, and the mixture was stirred in a hydrogenatmosphere at room temperature until no hydrogen was absorbed. Aftercompleting the reaction, Pd/C was removed, the solvent was distilledoff, and the residue was purified by a preparative column chromatographyusing a mixed solvent of heptane and toluene (heptane/toluene=4/1 byvolume) as a developing solvent and silica gel as a mediator, andfurther purified by recrystallization from a mixed solvent of heptaneand ethanol (heptane/ethanol=2/1 by volume) to obtain 9.1 g oftrans-4′-(2-(2-chloro-4-ethoxy-3-fluorophenyl)-ethyl)-trans-4-propyl-bicyclohexyl(C96). The resulting compound (C96) was colorless crystal, and the yieldwas 49.3% based on the compound (C67).

The transition temperatures of the resulting compound (C96) were asfollows.

Transition temperature: C 63.5 N 153.1 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified astrans-4′-(2-(2-chloro-4-ethoxy-3-fluorophenyl)-ethyl)-trans-4-propyl-bicyclohexyl.The measuring solvent was CDCl₃.

Chemical shift δ(ppm): 6.88 (dd, 1H), 6.79 (t, 1H), 4.08 (q, 2H), 2.65(t, 2H), 1.83-0.80 (m, 32H)

Example 8 Synthesis oftrans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4-vinyl-bicyclohexyl(C115)

First Step

4.8 g of well dried magnesium and 150 mL of THF were added to a reactorin a nitrogen atmosphere and heated to 47° C. 50.0 g of the compound(C2) dissolved in 50 mL of THF was added dropwise thereto slowly in atemperature range of 50 to 57° C., followed by stirring for 60 minutes.Thereafter, 39.2 g of a compound (b21) dissolved in 80 mL of THF wasadded dropwise thereto slowly in a temperature range of 47 to 58° C.,followed by stirring for 60 minutes. The resulting reaction mixture wascooled to 25° C. and then poured into 200 mL of a 13% ammonium chlorideaqueous solution and 500 mL of toluene. The resulting mixture was thenleft to rest to separate into an organic layer and an aqueous layer,followed by extracting to the organic layer. The resulting organic layerwas collected and washed with water, a 2N sodium hydroxide aqueoussolution, a saturated sodium hydrogen carbonate aqueous solution andwater, followed by drying over anhydrous magnesium sulfate. Thereafter,the solvent was distilled off under reduced pressure to obtain 84.7 g of1-(3-chloro-4-ethoxy-2-fluorophenyl)-4-(1,4-dioxa-spiro[4.5]dec-8-yl)cyclohexanol(b52).

Second Step

84.7 g of the compound (b52), 1.0 g of p-toluenesulfonic acid, 1.3 g ofethylene glycol and 320 mL of toluene were mixed, and the mixture wasrefluxed under heating for 2 hours while removing distilled water. Aftercooling the reaction mixture to 25° C., 300 mL of 3% sodium hydrogencarbonate aqueous solution and 200 mL of toluene was added to theresulting liquid, and the mixture was left at rest to separate into anorganic layer and an aqueous layer, followed by extracting to theorganic layer. The resulting organic layer was collected and washed witha 2N sodium hydroxide aqueous solution, a saturated sodium hydrogencarbonate aqueous solution and water, followed by drying over anhydrousmagnesium sulfate. Thereafter, the solvent was distilled off underreduced pressure to obtain a residue. The resulting residue was purifiedby a preparative column chromatography using toluene as a developingsolvent and silica gel as a mediator, and further purified byrecrystallization from a mixed solvent of heptane and toluene(heptane/toluene=2/1 by volume) to obtain 50.2 g of8-(4-(3-chloro-4-ethoxy-2-fluorophenyl)-cyclohexa-3-enyl)-1,4-dioxa-spiro[4.5]decane(b53). The yield was 77.3% based on the compound (b21).

Third Step

50.2 g of the compound (b53) was dissolved in a mixed solvent of 250 mLof toluene and 250 mL of isopropyl alcohol, to which 5.0 g of Raney-Niwas added, followed by stirring in a hydrogen atmosphere at roomtemperature until no hydrogen was absorbed. After completing thereaction, Raney-Ni was removed, and the solvent was distilled off toobtain 52.5 g of8-(4-(3-chloro-4-ethoxy-2-fluorophenyl)-cyclohexyl)-1,4-dioxa-spiro[4.5]decane(b54) as a crude material.

Fourth Step

52.5 g of the compound (b54) was dissolved in 250 mL of toluene, towhich 20.7 g of an 88% formic acid aqueous solution was added. Themixture was refluxed under heating for 6 hours. The reaction mixture wascooled to 25° C. and poured into a mixed solution of 300 mL of water and200 mL of toluene. They were mixed and then left at rest to separateinto an organic layer and an aqueous layer, followed by extracting tothe organic layer. The resulting organic layer was collected and washedwith a saturated sodium hydrogen carbonate aqueous solution and water,followed by drying over anhydrous magnesium sulfate. Thereafter, thesolvent was distilled off under reduced pressure to obtain a residue.The resulting residue was purified by recrystallization from a mixedsolvent of heptane and toluene (heptane/toluene=1/1 by volume) to obtain19.9 g of trans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-bicyclohexyl-4-one(b55). The yield was 44.4% based on the compound (b53)

Fifth Step

22.2 g of methoxymethyltriphenylphosphonium chloride was added to 60 mLof THF and cooled to −20° C. 7.0 g of potassium t-butoxide (t-BuOK) wasadded to the resulting mixed solution in a temperature range of −20 to−10° C., followed by stirring for 30 minutes. Thereafter, 19.0 g of thecompound (b55) dissolved in 40 mL of toluene was added dropwise theretoover 60 minutes in a temperature range of −15 to −5° C., followed bystirring for 30 minutes. After restoring the temperature of the reactionmixture to 0° C., a mixed solution of 100 mL of water and 200 mL oftoluene was poured thereto. They were mixed and then left at rest toseparate into an organic layer and an aqueous layer, followed byextracting to the organic layer. The resulting organic layer wascollected and washed with water, followed by drying over anhydrousmagnesium sulfate. Thereafter, the solvent was distilled off underreduced pressure to obtain a residue. The resulting residue was purifiedby a preparative column chromatography using a mixed solvent of heptaneand toluene (heptane/toluene=1/1 by volume) as a developing solvent andsilica gel as a mediator to obtain 20.1 g oftrans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-4-methoxymethylene-bicyclohexyl(b56). The yield was 98.0% based on the compound (b55).

Sixth Step

20.1 g of the compound (b56) was dissolved in 160 mL of THF, and themixture was stirred at 30° C. 40 mL of 3N hydrochloric acid was added tothe mixture, which was further stirred for 120 minutes. The resultingreaction mixture was poured into a mixed solution of 200 mL of water and300 mL of toluene. It was mixed and then left at rest to separate intoan organic layer and an aqueous layer, followed by extracting to theorganic layer. The resulting organic layer was collected and washed witha saturated sodium hydrogen carbonate aqueous solution and water,followed by drying over anhydrous magnesium sulfate. Thereafter, thesolvent was distilled off under reduced pressure to obtain 22.0 g of aresidue. 22.0 g of the resulting residue was dissolved in 60 mL oftoluene, and the resulting solution was poured into 240 mL of methanolhaving 0.2 g of sodium hydroxide dissolved therein, followed by stirringfor 3 hours at 5° C. The resulting reaction mixture was extracted with400 mL of toluene, and the resulting organic layer was washed withwater, followed by drying over anhydrous magnesium sulfate. Thereafter,the solvent was distilled off under reduced pressure to obtain 20.1 of aresidue. The residue was purified by recrystallization from a mixedsolvent of heptane and toluene (heptane/toluene=1/1 by volume) to obtain13.9 g oftrans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-bicyclohexyl-trans-4-carbaldehyde(b57). The yield was 71.9% based on the compound (b56).

Seventh Step

4.7 g of methyltriphenylphosphonium bromide was added to 20 mL of THFand cooled to 5° C. 1.4 g of potassium t-butoxide (t-BuOK) was added tothe resulting mixed solution in a temperature range of 5 to 10° C.,followed by stirring for 30 minutes. Thereafter, 4.0 g of the compound(b57) dissolved in 20 mL of toluene was added dropwise thereto over 30minutes in a temperature range of 5 to 10° C., followed by stirring for30 minutes. The reaction mixture was poured into a mixed solution of 50mL of water and 40 mL of toluene. They were mixed and then left at restto separate into an organic layer and an aqueous layer, followed byextracting to the organic layer. The resulting organic layer wascollected and washed with water, followed by drying over anhydrousmagnesium sulfate. Thereafter, the solvent was distilled off underreduced pressure to obtain a residue. The resulting residue was purifiedby a preparative column chromatography using a mixed solvent of heptaneand toluene (heptane/toluene=2/1 by volume) as a developing solvent andsilica gel as a mediator, and further purified by recrystallization froma mixed solvent of heptane and ethanol (heptane/ethanol=2/1 by volume)to obtain 3.2 g oftrans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4-vinyl-bicyclohexyl(C115). The yield was 79.4% based on the compound (b57).

The transition temperatures of the resulting compound (C115) were asfollows.

Transition temperature: C 113.4 N 151.9 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified astrans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4-vinyl-bicyclohexyl.The measuring solvent was CDCl₃.

Chemical shift δ(ppm): 7.03 (t, 1H), 6.66 (dd, 1H), 5.78 (m, 1H), 4.95(dt, 1H), 4.89 (dt, 1H), 4.08 (q, 2H), 2.73 (tt, 1H), 1.82 (m, 9H),1.47-1.37 (m, 5H), 1.21-1.10 (m, 8H)

Example 9 Synthesis of3-chloro-4-ethoxy-2-fluoro-4′-(trans-4-propyl-cyclohexyl)-biphenyl(C154)

First Step

4.79 g of well dried magnesium and 50 mL of THF were added to a reactorin a nitrogen atmosphere and heated to 50° C. 50.0 g of the compound(C2) dissolved in 200 mL of THF was added dropwise thereto over 60minutes in a temperature range of 43 to 48° C., followed by stirring for60 minutes. The resulting reaction mixture was cooled to 25° C.Thereafter, the reaction mixture was added dropwise to a solution of24.6 g of trimethyl borate and 100 mL of THF cooled to −50° C. over 60minutes in a nitrogen atmosphere in a temperature range of −60 to −40°C. The reaction mixture was warmed to 0° C. and then poured into 400 mLof 3N hydrochloric acid at 0° C. 700 mL of acetic acid was added to thesolution, followed by mixing, and the mixture was then left to rest toseparate into an organic layer and an aqueous layer, followed byextracting. The resulting organic layer was collected and washed with asaturated sodium hydrogen carbonate aqueous solution and water, followedby drying over anhydrous magnesium sulfate. Thereafter, the solvent wasdistilled off under reduced pressure to obtain a residue. The residuewas recrystallized from heptane. The recrystallization operation wasrepeated to obtain 35.9 g of 3-chloro-4-ethoxy-2-fluorophenylboronicacid (b58). The resulting compound (b58) was a yellowish solid.

Second Step

15.0 g of the compound (b58), 15 g of1-iodo-4-(trans-4-propylcyclohexyl)-benzene (b59), 19.0 g of potassiumcarbonate, 7.37 g of tetrabutylammonium bromide (TBAB) and 0.39 g ofPd/C were added to a reactor having 50 mL of toluene, 50 mL of SolmixA-11 and 2.5 mL of water placed therein. The mixture was refluxed underheating and stirring for 4 hours. After cooling the reaction mixture to25° C., potassium carbonate and Pd/C were filtered off. 100 mL oftoluene was added to the resulting solution, which was washed with a 2Nsodium hydroxide aqueous solution, a saturated sodium thiosulfateaqueous solution and water. Thereafter, the solvent was distilled offunder reduced pressure to obtain a residue. The residue was dissolved ina mixed solvent of ethyl acetate and Solmix A-11 (ethyl acetate/SolmixA-11=2/1 by volume) and recrystallized therefrom. The recrystallizationoperation was repeated to obtain 17.1 g of a yellowish solid. The solidwas dissolved in a mixed solvent of 80 mL of toluene and 20 mL of SolmixA-11, to which 0.5 g of Pd/C was added, followed by stirring for 15hours in a hydrogen atmosphere at 20° C. After removing Pd/C from thereaction mixture by filtration, the reaction mixture was washed with a2N sodium hydroxide aqueous solution, a saturated sodium thiosulfateaqueous solution and water, followed by drying over anhydrous magnesiumsulfate. Thereafter, the solvent was distilled off under reducedpressure to obtain a residue. The resulting residue was purified by apreparative column chromatography using a mixed solvent of heptane andtoluene (heptane/toluene=2/1 by volume) as a developing solvent andsilica gel as a mediator, and further purified by recrystallization froma mixed solvent of ethyl acetate and ethanol (ethyl acetate/ethanol=2/1by volume), followed by drying, to obtain 14.9 g of3-chloro-4-ethoxy-2-fluoro-4′-(trans-4-propyl-cyclohexyl)-biphenyl(C154). The resulting compound (C154) was colorless crystals, and theyield was 86.9% based on the compound (b59).

The transition temperatures of the resulting compound (C154) were asfollows.

Transition temperature: C 114.8 N 157.7 Iso The resulting compoundexhibited the following chemical shift δ(ppm) of ¹H-NMR analysis, andthus the compound was identified as3-chloro-4-ethoxy-2-fluoro-4′-(trans-4-propyl-cyclohexyl)-biphenyl. Themeasuring solvent was CDCl₃.

Chemical shift δ(ppm): 7.42 (d, 2H), 7.28-7.23 (m, 3H), 6.77 (dd, 1H),4.14 (q, 2H), 2.50 (tt, 1H), 1.94-0.89 (m, 19H)

Example 10 Synthesis of3-chloro-4-ethoxy-2-fluoro-4″-propyl-[1,1′;4′,1″]terphenyl (C195)

11.6 g of the compound (b58), 11.2 g of 4′-bromo-4-propyl-biphenyl(b60), 11.3 g of potassium carbonate and 0.29 g of Pd(PPh₃)₂Cl wereadded to a reactor having 110 mL of Solmix A-11 placed therein. Themixture was refluxed under heating and stirring for 9 hours. Aftercooling the reaction mixture to 25° C., potassium carbonate andPd(PPh₃)₂Cl were filtered off. 100 mL of toluene was added to theresulting solution, which was washed with a 2N sodium hydroxide aqueoussolution, a saturated sodium thiosulfate aqueous solution and water.Thereafter, the solvent was distilled off under reduced pressure toobtain a residue. The residue was recrystallized from ethyl acetate toobtain 5.5 g of a yellowish solid. The solid was dissolved in a mixedsolvent of 150 mL of toluene and 30 mL of Solmix A-11, to which 0.1 g ofPd/C was added, followed by stirring for 15 hours in a hydrogenatmosphere at 25° C. After removing Pd/C from the reaction mixture byfiltration, the filtrate was washed with a 2N sodium hydroxide aqueoussolution, a saturated sodium thiosulfate aqueous solution and water,followed by drying over anhydrous magnesium sulfate. Thereafter, thesolvent was distilled off under reduced pressure to obtain a residue.The resulting residue was purified by a preparative columnchromatography using a mixed solvent of heptane and ethyl acetate(heptane/ethyl acetate=1/1 by volume) as a developing solvent and silicagel as a mediator, and further purified by recrystallization from amixed solvent of toluene and ethanol (toluene/ethanol=1/1 by volume) toobtain 1.69 g of3-chloro-4-ethoxy-2-fluoro-4″-propyl-[1,1′;4′,1″]terphenyl (C195). Theresulting compound (C195) was colorless crystals, and the yield was11.2% based on the compound (b60).

The transition temperatures of the resulting compound (C195) were asfollows.

Transition temperature: C (129.2 S_(A)) 136.8 N 183.2 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified as3-chloro-4-ethoxy-2-fluoro-4″-propyl-[1,1′;4′,1″]terphenyl. Themeasuring solvent was CDCl₃.

Chemical shift δ(ppm): 7.66-7.54 (m, 6H), 7.28-7.25 (m, 3H), 6.80 (dd,1H), 4.16 (q, 2H), 2.64 (t, 2H), 1.72-1.63 (m, 2H), 1.50 (t, 3H), 0.98(t, 3H)

Example 11 Synthesis oftrans-4′-(3-chloro-4-ethoxy-2-fluorophenoxymethyl)-trans-4-propyl-bicyclohexyl(C232)

First Step

1.90 g of lithium aluminum hydride was suspended in 100 mL of THF. 60 mLof a THF solution having 20.01 g oftrans-4-(trans-4-propylcyclohexyl)cyclohexylaldehyde (b61) dissolvedtherein was added dropwise to the suspension liquid in a temperaturerange of 10 to 15° C., followed by stirring for 2 hours in thattemperature range. After completing the reaction, ethyl acetate and asaturated aqueous ammonium chloride were sequentially added to thereaction mixture under cooling with ice, and a deposit was removed byfiltering with Celite. The filtrate was extracted with ethyl acetate.The resulting organic layer was washed sequentially with water and asaturated sodium chloride aqueous solution, followed by drying overanhydrous magnesium sulfate. The solution was concentrated under reducedpressure to obtain 18.48 g of a crude compound containingtrans-4′-hydroxymethyl-trans-4-propyl-bicyclohexyl (b62). The resultingcrude compound was a colorless solid.

Second Step

18.48 g of the crude compound containing the compound (b62) and 26.68 gof triphenylphosphine were dissolved in 200 mL of methylene chloride.42.54 g of carbon tetrabromide was added dropwise to the solution slowlyat room temperature, followed by stirring for 5.5 hours at roomtemperature. A saturated sodium thiosulfate aqueous solution and ethylacetate were added to the crude compound, followed by mixing, and themixture was left at rest to separate into an organic layer and anaqueous layer, followed by extracting to the organic layer. Theresulting organic layer was washed sequentially with water and asaturated sodium chloride aqueous solution, dried over anhydrousmagnesium sulfate, and concentrated under reduced pressure to obtain aresidue. The residue was a yellowish solid. 74.77 g of the residue wassuspended in 300 mL of heptane, and after removing insoluble matters byfiltration, the filtrate was concentrated under reduced pressure toobtain 39.07 g of a residue in yellowish oily form. The residue waspurified by a preparative column chromatography using heptane as adeveloping solvent and silica gel as a mediator to obtain 24.36 g oftrans-4′-bromomethyl-trans-4-propyl-bicyclohexyl (b63). The resultingcompound (b63) was a colorless solid.

Third Step

30.02 g of the compound (C2) was dissolved in 300 mL of THF. sec-BuLi(1.01 M solution, 124 mL) was added dropwise to the resulting solutionin a temperature range of −70 to −75° C., and after completing thedropwise addition, the mixture was stirred for 1 hour in thattemperature range. 40 mL of a THF solution having 18.71 g triisopropylborate dissolved therein was added dropwise to the resulting solution ina temperature range of −70 to −75° C., and after completing the dropwiseaddition, the mixture was stirred for 1 hour in that temperature range.Thereafter, the temperature of the solution was gradually increased toroom temperature, followed by stirring over night. After adding 11.92 gof acetic acid to the reaction mixture, followed by stirring for 30minutes, 29.95 g of hydrogen peroxide was added dropwise thereto slowlyat room temperature, and after completing the dropwise addition, themixture was stirred for 4.5 hours at room temperature. A sodium nitriteaqueous solution and ethyl acetate were added to the reaction mixture,followed by mixing, and the mixture was left at rest to separate into anorganic layer and an aqueous layer, followed by extracting to theorganic layer. The resulting organic layer was washed sequentially withwater and a saturated sodium chloride aqueous solution, dried overanhydrous magnesium sulfate, and concentrated under reduced pressure toobtain a residue. The residue was a yellowish solid. 30.97 g of theresidue was purified by a preparative column chromatography using amixed solvent of heptane and ethyl acetate (heptane/ethyl acetate=5/1 byvolume) as a developing solvent and silica gel as a mediator to obtain13.29 g of 3-chloro-4-ethoxy-2-fluorophenol (b64). The resultingcompound (b64) was a yellowish solid.

Fourth Step

1.51 g of the compound (b64) obtained in the third step was dissolved in40 mL of N,N,-dimethylformamide. After suspending 1.99 g of potassiumcarbonate in the solution, 3.08 g of the compound (b63) obtained in thesecond step and 0.26 g of tetrabutylammonium bromide (TBAB) were addedthereto, followed by stirring for 17.5 hours at 80° C. After completingthe reaction, water and ethyl acetate were added to the reactionmixture, followed by mixing, and the mixture was left at rest toseparate into an organic layer and an aqueous layer, followed byextracting to the organic layer. The resulting organic layer was washedsequentially with water, a 5% sodium thiosulfate aqueous solution, waterand a saturated sodium chloride aqueous solution, dried over anhydrousmagnesium sulfate, and concentrated under reduced pressure to obtain aresidue. The residue was a colorless solid. 3.56 g of the residue waspurified by a preparative column chromatography using a mixed solvent ofheptane and ethyl acetate (heptane/ethyl acetate=50/1 by volume) as adeveloping solvent and silica gel as a mediator, and further purified byrepeating recrystallization from a mixed solvent of heptane and ethanol(heptane/ethanol=1/1 by volume) to obtain purifiedtrans-4′-(3-chloro-4-ethoxy-2-fluorophenoxymethyl)-trans-4-propyl-bicyclohexyl(C232).

The transition temperatures of the resulting compound (C232) were asfollows.

Transition temperature: C 80.1 N 139.9 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified astrans-4′-(3-chloro-4-ethoxy-2-fluorophenoxymethyl)-trans-4-propyl-bicyclohexyl.The measuring solvent was CDCl₃.

Chemical shift δ(ppm): 6.58-6.66 (m, 2H), 4.06 (q, 2H), 3.76 (d, 2H),1.94-0.85 (m, 30H)

Example 12 Synthesis of3-chloro-2-fluoro-4-(trans-4-pentyl-cyclohexylmethoxy)-4′-propylbiphenyl(C264)

First Step

24.7 g of the compound (b65), 30.0 g of1-bromo-3-chloro-2-fluoro-4-methoxybenzene (C1), 34.6 g of potassiumcarbonate and 0.88 g of Pd(PPh₃)₂Cl were added to a reactor having 120mL of Solmix A-11 placed therein. The mixture was refluxed under heatingand stirring for 2 hours. After cooling the reaction mixture to 30° C.,200 mL of toluene and 300 mL of water were added to the reactionmixture, followed by mixing. Thereafter, the mixture was left at rest toseparate into an organic layer and an aqueous layer, followed byextracting to the organic layer. The resulting organic layer was washedsequentially with a 2N sodium hydroxide aqueous solution, a saturatedsodium hydrogen carbonate aqueous solution and water. Thereafter, thesolvent was distilled off under reduced pressure to obtain a residue.The residue was recrystallized from Solmix A-11 to obtain 28.4 g of ayellowish solid. The solid was dissolved in a mixed solvent of 100 mL oftoluene and 30 mL of Solmix A-11, to which 0.5 g of Pd/C was added,followed by stirring for 20 hours in a hydrogen atmosphere at 25° C.After removing Pd/C from the reaction mixture by filtration, the solventwas distilled off under reduced pressure to obtain a residue. Theresulting residue was purified by a preparative column chromatographyusing a heptane as a developing solvent and silica gel as a mediator,and further purified by recrystallization from Solmix A-11 to obtain24.9 g of 3-chloro-2-fluoro-4-methoxy-4′-propylbiphenyl (b66). Theresulting compound (b66) was colorless crystals, and the yield was 71.2%based on the compound (C1).

The transition temperature of the resulting compound (b66) was asfollows.

Transition temperature: C 54.1 Iso

Second Step

22.0 g of the compound (b66) was dissolved in 200 mL of methylenechloride. 23.7 g of boron tribromide was added dropwise to the resultingsolution in a temperature range of −27 to −20° C., and the temperatureof the solution was gradually increased to room temperature, followed bystirring over night. The resulting reaction mixture was poured slowly to300 mL of iced water, and the mixture was left at rest to separate intoan organic layer and an aqueous layer, followed by extracting to theorganic layer. The resulting organic layer was washed with a sodiumchloride aqueous solution in three times, dried over anhydrous magnesiumsulfate, and concentrated under reduced pressure to obtain a residue.The residue was a yellowish solid. 19.7 g of the residue was purified byrecrystallization from a mixed solvent of heptane and toluene(heptane/toluene=2/1 by volume) to obtain 18.0 g of3-chloro-2-fluoro-4′-propylbiphenyl-4-ol (b67). The resulting compound(b67) was a white solid.

Third Step

4.0 g of the compound (b67) obtained in the second step was dissolved in20 mL of N,N,-dimethylformamide. After suspending 2.5 g of potassiumcarbonate in the solution, 5.6 g of the compound (b68) was addedthereto, followed by stirring for 6 hours at 70° C. After completing thereaction, water and toluene were added to the reaction mixture, followedby mixing. Thereafter, the mixture was left at rest to separate into anorganic layer and an aqueous layer, followed by extracting to theorganic layer. The resulting organic layer was washed sequentially withwater, a 2N sodium hydroxide aqueous solution, a saturated sodiumchloride aqueous solution and water, and then concentrated under reducedpressure to obtain a residue. 7.7 g of the residue was purified by apreparative column chromatography using a mixed solvent of heptane andtoluene (heptane/toluene=3/1 by volume) as a developing solvent andsilica gel as a mediator, and further purified by repeatingrecrystallization from a mixed solvent of heptane and Solmix A-11(heptane/Solmix A-11=2/1 by volume) to obtain3-chloro-2-fluoro-4-(trans-4-pentyl-cyclohexylmethoxy)-4′-propylbiphenyl(C264) as colorless crystals. The yield was 89.5% based on the compound(b67).

The transition temperatures of the resulting compound (C264) were asfollows.

Transition temperature: C 79.9 N 110.6 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified as3-chloro-2-fluoro-4-(trans-4-pentyl-cyclohexylmethoxy)-4′-propylbiphenyl(C264). The measuring solvent was CDCl₃.

Chemical shift δ(ppm): 7.41-7.39 (m, 2H), 7.25-7.22 (m, 3H), 6.77-6.75(dd, 1H), 3.85 (d, 2H), 2.63 (t, 2H), 1.94 (m, 2H), 1.85-1.81 (m, 3H),1.68 (m, 2H), 1.31-1.06 (m, 11H), 1.10-0.85 (m, 8H)

Example 13 Synthesis of3′-chloro-4″-ethyl-2′-fluoro-4-propyl-[1,1′;4′,1″]terphenyl (C293)

First Step

13.0 g of the compound (b67) was added to a reactor having 50 mLpyridine placed therein in a nitrogen atmosphere, and after dissolving,the solution was cooled to 5° C. 16.6 g of trifluoromethanesulfonicanhydride was added dropwise to the solution over 1 hour in atemperature range of 5 to 10° C., followed by stirring for 3 hour at 20°C. The resulting reaction mixture was poured slowly into a cooled mixedsolution of 100 mL of 1N hydrochloric acid and 100 mL of heptane.Thereafter, the mixture was left at rest to separate into an organiclayer and an aqueous layer, followed by extracting to the organic layer.The resulting organic layer was washed sequentially with water, asaturated sodium hydrogen carbonate aqueous solution and water. Theresulting organic layer was purified by a preparative columnchromatography using heptane as a developing solvent and silica gel as amediator, and then the solvent was distilled off under reduced pressureto obtain 19.1 g of a colorless transparent compound (b69). The yieldwas 97.9% based on the compound (b67).

Second Step

6.0 g of the compound (b69) 2.7 g of the compound (b70), 9.6 g oftripotassium phosphate, 2.44 g of TBAB, 0.49 g of zinc powder and 0.11 gof Pd(PPh₃)₂Cl were added to a reactor having 60 mL of 1,4-dioxane in anitrogen atmosphere. They were stirred for 4 hours under refluxing byheating. 2.0 g of tripotassium phosphate was further added thereto, andthe mixture was stirred for 2 hours under refluxing by heating. Aftercooling the resulting reaction mixture to 30° C., the resulting reactionmixture was poured slowly into a mixed solution of 100 mL of toluene and200 mL of 1N hydrochloric acid. Thereafter, the mixture was left at restto separate into an organic layer and an aqueous layer, followed byextracting to the organic layer. The resulting organic layer was washedsequentially with 1N hydrochloric acid, a 2N sodium hydroxide aqueoussolution, a saturated sodium hydrogen carbonate aqueous solution andwater. Thereafter, the solvent was distilled off to obtain 5.3 g ofresidue. The residue was purified by a preparative column chromatographyusing a mixed solvent of heptane and toluene (heptane/toluene=4/1 byvolume) as a developing solvent and silica gel as a mediator, andfurther purified by repeating recrystallization from a mixed solvent ofheptane and ethanol (heptane/ethanol=2/1 by volume) to obtain 3.9 g of3′-chloro-4″-ethyl-2′-fluoro-4-propyl-[1,1′;4′,1″]terphenyl (C293) ascolorless crystals. The yield was 72.3% based on the compound (b69).

The transition temperature of the resulting compound (C293) was asfollows.

Transition temperature: C 83.4 Iso

The resulting compound exhibited the following chemical shift δ(ppm) of¹H-NMR analysis, and thus the compound was identified as3′-chloro-4″-ethyl-2′-fluoro-4-propyl-[1,1′;4′,1″]terphenyl (C293). Themeasuring solvent was CDCl₃.

Chemical shift δ(ppm): 7.50-7.49 m, 2H), 7.42-7.40 (m, 2H), 7.36 (t,1H), 7.29 (t, 4H), 7.19 (dd, 1H), 2.73 (q, 2H), 2.65 (t, 2H), 1.70 (m,2H), 1.30 (t, 3H), 0.99 (t, 3H)

Example 14

The following compounds (C21) to (C27), (C29) to (C43), (C45) to (C57),(C59) to (C95), (C97) to (C114), (C116) to (C153), (C155) to (C194),(C196) to (C231), (C233) to (C263), (C265) to (C292), and (C294) to(C300) were synthesized in the similar manner as the synthesis methodsdescribed in Examples 4 to 13. The compounds (C28), (C44), (C58), (C96),(C15), (C154), (C195), (C232), (C264) and (C293) are also described inthe following. The values shown with the compounds are values measuredin the aforementioned methods, in which the maximum temperature(T_(NI)), the dielectric anisotropy (Δ∈) and the optical anisotropy (Δn)are extrapolated values obtained by converting measured values ofsamples obtained by mixing the compound with the base mixture A, bymeans of the aforementioned extrapolation method.

Example 15 Characteristics of Liquid Crystal Compound (C28)

The five compounds having been described as the base mixture A weremixed to prepare mother liquid crystal A having a nematic phase. Thebase mixture A had the following characteristics.

Maximum temperature (T_(NI))=74.0° C.; Viscosity (η₂₀)=18.9 mPa·s;Optical anisotropy (Δn)=0.087; Dielectric anisotropy (Δ∈)=−1.3

A liquid crystal composition B containing 85% by weight of the basemixture A and 15% by weight oftrans-4′-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4-propyl-bicyclohexyl(C28) obtained in Example 4 was prepared. The characteristics of theliquid crystal composition B were measured, and the characteristics wereas follows.

Maximum temperature (T_(NI))=85.4° C.; Optical anisotropy (Δn)=0.090;Dielectric anisotropy (Δ∈)=−1.97

The liquid crystal composition B was stored at −10° C., and itmaintained a nematic phase for 20 days. Since the maximum temperature(T_(NI)) was largely increased, and the dielectric anisotropy (Δ∈) wasnegatively increased by adding the liquid crystal compound (C28) to thebase mixture A, it was found that the liquid crystal compound (C28)contributed to enhancement of the temperature range of a nematic phase,and a liquid crystal display device having as a constitutional element aliquid crystal composition containing the compound could be driven at alow voltage.

Since the liquid crystal composition B maintained a nematic phase for 20days even when stored at −10° C., it was found that the liquid crystalcompound (C28) was excellent in compatibility at a low temperature.

Example 16 Characteristics of Liquid Crystal Compound (C58)

A liquid crystal composition C containing 85% by weight of the basemixture A described in Example 15 and 15% by weight oftrans-4′-(2-(3-chloro-4-ethoxy-2-fluorophenyl)-vinyl)-trans-4-propyl-bicyclohexyl(C58) obtained in Example 6 was prepared. The characteristics of theliquid crystal composition C were measured, and the characteristics wereas follows.

Maximum temperature (T_(NI))=93.0° C.; Optical anisotropy (Δn)=0.096;Dielectric anisotropy (Δ∈)=−2.07

The liquid crystal composition C was stored at −10° C., and itmaintained a nematic phase for 30 days. Since the maximum temperature(T_(NI)) was largely increased, and the dielectric anisotropy (Δ∈) wasnegatively increased by adding the liquid crystal compound (C58) to thebase mixture A, it was found that the liquid crystal compound (C58)contributed to enhancement of the temperature range of a nematic phase,and a liquid crystal display device having as a constitutional element aliquid crystal composition containing the compound could be driven at alow voltage.

Since the liquid crystal composition C maintained a nematic phase for 30days even when stored at −10° C., it was found that the liquid crystalcompound (C58) was excellent in compatibility at a low temperature.

Example 17 Characteristics of Liquid Crystal Compound (C96)

A liquid crystal composition D containing 85% by weight of the basemixture A described in Example 15 and 15% by weight oftrans-4′-(2-(2-chloro-4-ethoxy-3-fluorophenyl)-ethyl)-trans-4-propyl-bicyclohexyl(C96) obtained in Example 7 was prepared. The characteristics of theliquid crystal composition D were measured, and the characteristics wereas follows.

Maximum temperature (T_(NI))=85.1° C.; Optical anisotropy (Δn)=0.089;Dielectric anisotropy (Δ∈)=−1.90

The liquid crystal composition D was stored at −10° C., and itmaintained a nematic phase for 30 days. Since the maximum temperature(T_(NI)) was largely increased, and the dielectric anisotropy (Δ∈) wasnegatively increased by adding the liquid crystal compound (C96) to thebase mixture A, it was found that the liquid crystal compound (C96)contributed to enhancement of the temperature range of a nematic phase,and a liquid crystal display device having as a constitutional element aliquid crystal composition containing the compound could be driven at alow voltage.

Since the liquid crystal composition D maintained a nematic phase for 30days even when stored at −10° C., it was found that the liquid crystalcompound (C96) was excellent in compatibility at a low temperature.

Example 18 Characteristics of Liquid Crystal Compound (C116)

A liquid crystal composition E containing 85% by weight of the basemixture A described in Example 15 and 15% by weight oftrans-4-(3-chloro-4-ethoxy-2-fluorophenyl)-trans-4′-propenylbicyclohexyl(C116) obtained in Example 14 was prepared. The characteristics of theliquid crystal composition E were measured, and the characteristics wereas follows.

Maximum temperature (T_(NI))=87.6° C.; Optical anisotropy (Δn)=0.092;Dielectric anisotropy (Δ∈)=−2.08

Since the maximum temperature (T_(NI)) was largely increased, and thedielectric anisotropy (Δ∈) was negatively increased significantly byadding the liquid crystal compound (C116) to the base mixture A, it wasfound that the liquid crystal compound (C116) contributed to enhancementof the temperature range of a nematic phase, and a liquid crystaldisplay device having as a constitutional element a liquid crystalcomposition containing the compound could be driven at a significantlylow voltage.

Example 19 Characteristics of Liquid Crystal Compound (C158)

A liquid crystal composition F containing 85% by weight of the basemixture A described in Example 15 and 15% by weight of4-butoxy-3-chloro-2-fluoro-trans-4′-(trans-4-propylcyclohexyl)biphenyl(C158) obtained in Example 14 was prepared. The characteristics of theliquid crystal composition F were measured, and the characteristics wereas follows.

Maximum temperature (T_(NI))=83.3° C.; Optical anisotropy (Δn)=0.097;Dielectric anisotropy (Δ∈)=−1.95

The liquid crystal composition F was stored at −10° C., and itmaintained a nematic phase for 30 days. Since the maximum temperature(T_(NI)) was largely increased, and the dielectric anisotropy (Δ∈) wasnegatively increased by adding the liquid crystal compound (C158) to thebase mixture A, it was found that the liquid crystal compound (C158)contributed to enhancement of the temperature range of a nematic phase,and a liquid crystal display device having as a constitutional element aliquid crystal composition containing the compound could be driven at alow voltage.

Since the liquid crystal composition F maintained a nematic phase for 30days even when stored at −10° C., it was found that the liquid crystalcompound (C158) was excellent in compatibility at a low temperature.

Example 20 Characteristics of Liquid Crystal Compound (C247)

A liquid crystal composition G containing 85% by weight of the basemixture A described in Example 15 and 15% by weight oftrans-4′-(2-chloro-4-ethoxy-3-fluorophenoxymethyl)-trans-4-propylbicyclohexyl(C247) obtained in Example 14 was prepared. The characteristics of theliquid crystal composition G were measured, and the characteristics wereas follows.

Maximum temperature (T_(NI))=84.0° C.; Optical anisotropy (Δn)=0.089;Dielectric anisotropy (Δ∈)=−2.27

The liquid crystal composition G was stored at −10° C., and itmaintained a nematic phase for 30 days. Since the maximum temperature(T_(NI)) was largely increased, and the dielectric anisotropy (Δ∈) wasnegatively increased by adding the liquid crystal compound (C247) to thebase mixture A, it was found that the liquid crystal compound (C247)contributed to enhancement of the temperature range of a nematic phase,and a liquid crystal display device having as a constitutional element aliquid crystal composition containing the compound could be driven at alow voltage.

Since the liquid crystal composition G maintained a nematic phase for 30days even when stored at −10° C., it was found that the liquid crystalcompound (C247) was excellent in compatibility at a low temperature.

Comparative Example 1

As a comparative compound 1,trans-4-(2,3-difluoro-4-ethoxyphenyl)-trans-4′-propylbicyclohexylreported in JP H2-503441 A/1990 (Compound (A) described hereinabove) wassynthesized.

A liquid crystal composition H containing 85% by weight of the basemixture A described in Example 15 and 15% by weight of the comparativecompound 1 was prepared. The characteristics of the liquid crystalcomposition H were measured, and the characteristics were as follows.

Maximum temperature (T_(NI))=86.7° C.; Optical anisotropy (Δn)=0.091;Dielectric anisotropy (Δ∈)=−1.92

The liquid crystal composition H was stored at −10° C., and it wasconfirmed that crystals were deposited on the seventh day.

Accordingly, it was found from the comparison between the comparativecompound 1 and the compound (C28) shown in Example 15 that the compoundof the invention is excellent in compatibility at a low temperaturealthough these compounds are equivalent in maximum temperature (T_(NI))and dielectric anisotropy (Δ∈).

Comparative Example 2

As a comparative compound 2,2-chloro-1-ethoxy-3-fluoro-4-(trans-4-propylcyclohexyl)benzene reportedin WO 98/23561 A/1998 was synthesized.

The comparative compound 2 was measured for transition temperature, andit was C 59.4 Iso. It was thus found that the compound did not have anematic phase as useful characteristics of a compound necessary for aliquid crystal display device.

A liquid crystal composition I containing 85% by weight of the basemixture A described in Example 15 and 15% by weight of the comparativecompound 2 was prepared. The characteristics of the liquid crystalcomposition I were measured, and the characteristics were as follows.

Maximum temperature (T_(NI))=63.5° C.; Optical anisotropy (Δn)=0.084;Dielectric anisotropy (Δ∈)=−1.98

Since the maximum temperature (T_(NI)) was largely decreased by addingthe comparative compound 2 to the base mixture A, it was found that thecomparative compound 2 did not contribute to enhancement of thetemperature range of a nematic phase, and was not a compound capable ofderiving characteristics necessary of a liquid crystal display device.

Comparative Example 3

As a comparative compound 3,trans-4-(2,3-dichloro-4-ethoxyphenyl)-trans-4′-propylbicyclohexyl wassynthesized.

A liquid crystal composition J containing 85% by weight of the basemixture A described in Example 15 and 15% by weight of the comparativecompound 3 was prepared. The characteristics of the liquid crystalcomposition J were measured, and the characteristics were as follows.

Optical anisotropy (Δn)=0.088; Dielectric anisotropy (Δ∈)=−1.60

It was found from the comparison between the comparative compound 3 andthe compound (C28) shown in Example 15 that the compound of theinvention is excellent in dielectric anisotropy.

Comparative Example 4 Composition K

The composition K shown below was prepared.

The characteristics of the liquid crystal composition K were measured,and the characteristics were as follows.

Maximum temperature (T_(NI))=68.9° C.; Optical anisotropy (Δn)=0.081;Dielectric anisotropy (Δ∈)=−3.26

The liquid crystal composition K was stored at temperatures of −10° C.and −20° C. for 30 days, and it was confirmed that crystals weredeposited at both temperatures of −10° C. and −20° C.

Example 21 Composition L

The composition L shown below was prepared.

The characteristics of the liquid crystal composition L were measured,and the characteristics were as follows.

Maximum temperature (T_(NI))=63.9° C.; Optical anisotropy (Δn)=0.077;Dielectric anisotropy (Δ∈)=−3.1

The liquid crystal composition L was stored at temperatures of −10° C.and −20° C. for 30 days, and it was confirmed that crystals weredeposited at −20° C., but no crystal was deposited and it maintained anematic phase at −10° C.

In the liquid crystal composition L, the optical anisotropy (Δn) couldbe small, and the minimum temperature of a nematic phase could beenhanced, as compared to the composition K in Comparative Example 4.

Example 22 Composition M

The composition M shown below was prepared.

The characteristics of the liquid crystal composition M were measured,and the characteristics were as follows.

Maximum temperature (T_(NI))=59.3° C.; Optical anisotropy (Δn)=0.073;Dielectric anisotropy (Δ∈)=−3.1

The liquid crystal composition M was stored at temperatures of −10° C.and −20° C. for 30 days, and it was confirmed that no crystal wasdeposited and it maintained a nematic phase at both temperatures of −20°C. and −10° C.

In the liquid crystal composition L, the optical anisotropy (Δn) couldbe small, and the minimum temperature of a nematic phase could beenhanced, as compared to the composition K in Comparative Example 4.

Example 23 Composition N

The composition N shown below was prepared.

The characteristics of the liquid crystal composition N were measured,and the characteristics were as follows.

Maximum temperature (T_(NI))=58.3° C.; Optical anisotropy (Δn)=0.074;Dielectric anisotropy (Δ∈)=−2.9

The liquid crystal composition N was stored at temperatures of −10° C.,−20° C. and −30° C. for 30 days, and it was confirmed that no crystalwas deposited and it maintained a nematic phase at all temperatures of−10° C., −20° C. and −30° C.

In the liquid crystal composition N, the optical anisotropy (Δn) couldbe small, and the minimum temperature of a nematic phase could beenhanced, as compared to the composition K in Comparative Example 4.

Example 24 Composition O

The composition O shown below was prepared.

The characteristics of the liquid crystal composition O were measured,and the characteristics were as follows.

Maximum temperature (T_(NI))=70.0° C.; Optical anisotropy (Δn)=0.078;Dielectric anisotropy (Δ∈)=−3.4

The liquid crystal composition O was stored at temperatures of −10° C.and −20° C. for 30 days, and it was confirmed that crystals weredeposited at −20° C., but no crystal was deposited and it maintained anematic phase at −10° C.

In the liquid crystal composition O, the maximum temperature (T_(NI))was high, and the minimum temperature of a nematic phase could beenhanced, as compared to the composition K in Comparative Example 4, andtherefore, the liquid crystal composition O could be used in a widetemperature range. In the liquid crystal composition O, the dielectricanisotropy (Δ∈) is negatively large, and a liquid crystal display devicehaving as a constitutional element the liquid crystal composition couldbe driven at a low voltage.

1. A liquid crystal compound represented by one of formulas (b) to (d):

wherein Ra and Rb are independently hydrogen or linear alkyl having 1 to10 carbons, provided that in the alkyl, —CH₂— may be replaced by —O—,—(CH₂)₂— may be replaced by —CH═CH—; rings A¹, A² and B areindependently trans-1,4-cyclohexylene or 1,4-phenylene, ring C is1,4-phenylene; Z¹¹, Z¹², Z² and Z³ are independently a single bond oralkylene having 2 or 4 carbons, provided that in the alkylene, —CH₂— maybe replaced by —O— and —(CH₂)₂— may be replaced by —CH═CH—; and X₁ ischlorine, and X₂ is flourine, provided that: in a case where: in formula(b), rings A¹ and B are trans-1,4-cyclohexylene, Z¹¹ is a single bond,and Z² is —CH₂O—, in formula (c), ring A¹ is trans-1,4-cyclohexylene,ring B is 1,4-phenylene, Z¹¹, Z² and Z³ are a single bond, and informula (d), rings A¹, A² and B are trans-1,4-cyclohexylene, Z¹¹ and Z¹²are a single bond, and Z² is a single bond or —CH₂O—, Rb is one oflinear alkoxy having 1 to 9 carbons, linear alkoxyalkyl having 2 to 9carbons, linear alkenyl having 2 to 10 carbons, and linear alkenyloxyhaving 2 to 9 carbons, and in formula (b), ring A¹ and B aretrans-1,4-cyclohexylene, Z¹¹ is —CH₂O— and, Z² is a single bond, Rb isone of linear alkyl having 1 to 10 carbons, linear alkenyl having 2 to10 carbons, and linear alkenyloxy having 2 to 9 carbons.
 2. A liquidcrystal compound represented by one of formulas (b-1) to (d-1):

wherein Ra₁ and Rb₁ are independently linear alkyl having 1 to 10carbons, provided that in the alkyl, —CH₂— may be replaced by —O—,—(CH₂)₂— may be replaced by —CH═CH; rings A¹, A² and B are independentlytrans-1,4-cyclohexylene or 1,4-phenylene; Z¹¹, Z¹², Z² and Z³ areindependently a single bond or alkylene having 2 or 4 carbons, providedthat in the alkylene, —CH₂— may be replaced by —O— and —(CH₂)₂— may bereplaced by —CH═CH—; and X₁ is chlorine, and X₂ is fluorine, providedthat: in a case where: in formula (b-1), rings A¹ and B aretrans-1,4-cyclohexylene, Z¹¹ is a single bond, and Z² is —CH₂O—, and informula (d-1), rings A¹, A² and B are trans-1,4-cyclohexylene, Z¹¹ andZ¹² are a single bond, and Z² is a single bond or —CH₂O—, Rb₁ is one oflinear alkoxy having 1 to 9 carbons, linear alkoxyalkyl having 2 to 9carbons, linear alkenyl having 2 to 10 carbons, and linear alkenyloxyhaving 2 to 9 carbons, and in formula (b-1), rings A¹ and B aretrans-1,4-cyclohexylene, Z¹¹ is —CH₂O—, and Z² is a single bond, Rb₁ isone of linear alkyl having 1 to 10 carbons, linear alkenyl having 2 to10 carbons, and linear alkenyloxy having 2 to 9 carbons.
 3. A liquidcrystal compound represented by one of formulas (b-2-1) to (b-7-1):

wherein Ra₂ is linear alkyl having 1 to 10 carbons or linear alkenylhaving 2 to 10 carbons, Rb₂ is linear alkyl having 1 to 10 carbons orlinear alkoxy having 1 to 9 carbons, and the cyclohexylene ring istrans-1,4-cyclohexylene.
 4. The liquid crystal compound according toclaim 3, wherein the compound represented by one of formulas (b-2-1) to(b-7-1), wherein Ra₂ is linear alkyl having 1 to 10 carbons, and Rb₂ islinear alkoxy having 1 to 9 carbons.
 5. A liquid crystal compoundrepresented by one of formulas (b-8-1) to (b-10-1):

wherein Ra₃ is linear alkyl having 1 to 10 carbons or linear alkenylhaving 2 to 10 carbons, Rb₃ is linear alkoxy having 1 to 9 carbons, andthe cyclohexylene ring is trans-1,4-cyclohexylene.
 6. The liquid crystalcompound according to claim 5, wherein the compound represented by oneof formulas (b-8-1) to (b-10-1), wherein Ra₃ is linear alkyl having 1 to10 carbons.
 7. A liquid crystal composition comprising the liquidcrystal compound according to claim
 1. 8. A liquid crystal displaydevice comprising a liquid crystal composition comprising the liquidcrystal compound according to claim
 1. 9. A liquid crystal compoundrepresented by one of formulas (b-2) to (d-2):

wherein Ra₁ and Rb₁ is linear alkyl having 1 to 10 carbons, providedthat in the alkyl, —CH₂— may be replaced by —O—, —(CH₂)₂— may bereplaced by —CH═CH—; rings A¹, A² and B are independentlytrans-1,4-cyclohexylene or 1,4-phenylene, ring C is 1,4-phenylene; Z¹¹is a single bond or —(CH₂)₂—, Z¹², Z² and Z³ are independently a singlebond or alkylene having 2 or 4 carbons, provided that in the alkylene,—CH₂— may be replaced by —O— and —(CH₂)₂— may be replaced by —CH═CH—;and X₁ is chlorine, and X₂ is flourine, provided that: in a case where:in formula (b-2), rings A¹ and B are trans-1,4-cyclohexylene, Z¹¹ is asingle bond, and Z² is —CH₂O—, and in formula (d-2), rings A¹, A² and Bare trans-1,4-cyclohexylene, Z¹¹ and Z¹² are a single bond, and Z² is asingle bond or —CH₂O—, Rb₁ is one of linear alkoxy having 1 to 9carbons, linear alkoxyalkyl having 2 to 9 carbons, linear alkenyl having2 to 10 carbons, and linear alkenyloxy having 2 to 9 carbons.
 10. Theliquid crystal compound according to claim 9, wherein the compoundrepresented by formula (b-2), wherein Ra₁ and Rb₁ are independentlylinear alkyl having 1 to 10 carbons, linear alkoxy having 1 to 9carbons, linear alkoxyalkyl having 1 to 9 carbons, linear alkenyl having2 to 10 carbons, or linear alkenyloxy having 2 to 9 carbons, Z¹¹ is asingle bond or —(CH₂)₂— and Z¹², Z² and Z³ are independently a singlebond, —(CH₂)₂—, —CH═CH—, —CH₂O— or —OCH₂—.
 11. The liquid crystalcompound according to claim 9, wherein the compound represented byformula (c-2) or (d-2), wherein Ra₁ and Rb₁ are independently linearalkyl having 1 to 10 carbons, linear alkoxy having 1 to 9 carbons,linear alkoxyalkyl having 1 to 9 carbons, or linear alkenyl having 2 to10 carbons, and Z¹¹ is a single bond or —(CH₂)₂— and Z¹², Z² and Z³ areindependently a single bond, —(CH₂)₂—, —CH═CH—, —CH₂O— or —OCH₂—. 12.The liquid crystal compound according to claim 9, wherein the compoundrepresented by one of formulas (b-2) to (d-2), wherein Ra₁ is linearalkyl having 1 to 10 carbons or linear alkenyl having 2 to 10 carbons,Rb₁ is linear alkyl having 1 to 10 carbons or linear alkoxy having 1 to9 carbons; Z¹¹ is a single bond or —(CH₂)₂— and Z¹², Z² and Z³ areindependently a single bond, —(CH₂)₂—, —CH═CH—, —CH₂O— or —OCH₂—. 13.The liquid crystal compound according to claim 9, wherein the compoundrepresented by one of formulas (b-2) to (d-2), wherein Z¹¹ is a singlebond or —(CH₂)₂— and Z¹², Z² and Z³ are independently a single bond,—(CH₂)₂— or —CH═CH—.
 14. The liquid crystal compound according to claim9, wherein the compound represented by one of formulas (b-2) to (d-2),wherein Ra₁ is linear alkyl having 1 to 10 carbons or linear alkenylhaving 2 to 10 carbons, Rb₁ is linear alkoxy having 1 to 9 carbons, Z¹¹is a single bond or —(CH₂)₂— and Z¹² and Z³ are independently a singlebond, —(CH₂)₂—, —CH═CH—, —CH₂O— or —OCH₂—, and Z² is —CH₂O—.